An anti-infective agent most commonly used in the treatment of urinary tract infections. Its anti-infective action derives from the slow release of formaldehyde by hydrolysis at acidic pH. (From Martindale, The Extra Pharmacopoeia, 30th ed, p173)
A local anesthetic that has been used in urinary tract disorders. Its use is limited by problems with toxicity (primarily blood disorders) and potential carcinogenicity.
A genus of ascomycetous FUNGI, family Pneumocystidaceae, order Pneumocystidales. It includes various host-specific species causing PNEUMOCYSTIS PNEUMONIA in humans and other MAMMALS.
A pulmonary disease in humans occurring in immunodeficient or malnourished patients or infants, characterized by DYSPNEA, tachypnea, and HYPOXEMIA. Pneumocystis pneumonia is a frequently seen opportunistic infection in AIDS. It is caused by the fungus PNEUMOCYSTIS JIROVECII. The disease is also found in other MAMMALS where it is caused by related species of Pneumocystis.
The marking of biological material with a dye or other reagent for the purpose of identifying and quantitating components of tissues, cells or their extracts.
Inflammation of the URINARY BLADDER, either from bacterial or non-bacterial causes. Cystitis is usually associated with painful urination (dysuria), increased frequency, urgency, and suprapubic pain.
Symptoms of disorders of the lower urinary tract including frequency, NOCTURIA; urgency, incomplete voiding, and URINARY INCONTINENCE. They are often associated with OVERACTIVE BLADDER; URINARY INCOMPETENCE; and INTERSTITIAL CYSTITIS. Lower urinary tract symptoms in males were traditionally called PROSTATISM.
Presence of blood in the urine.
A species of POLYOMAVIRUS apparently infecting over 90% of children but not clearly associated with any clinical illness in childhood. The virus remains latent in the body throughout life and can be reactivated under certain circumstances.
Abnormalities in the process of URINE voiding, including bladder control, frequency of URINATION, as well as the volume and composition of URINE.
A musculomembranous sac along the URINARY TRACT. URINE flows from the KIDNEYS into the bladder via the ureters (URETER), and is held there until URINATION.
Bleeding or escape of blood from a vessel.

Prophylactic chemotherapy with low-dosage trimethoprim-sulfamethoxazole following acute urinary tract infections in children. (1/45)

The cases of 10 children with acute and recurrent infection of the urinary tract are presented. Their ages were between 7 weeks and 9 years. Five of the children had been previously treated with a combination of sulfisoxazole, ampicillin, mandelamine and nitrofurantion and four of these children had "breakthrough" infections. When trimethoprim-sulfamethoxazole was administered twice weekly no further infections were noted in four of these five patients. The second group of five children were started on trimethoprim-sulfamethoxazole from the start of their infection and treatment was continued twice weekly for 5 to 7 months. No recurrence of infection of the urine has been detected up to the present time. It is concluded that treatment with trimethoprim-sulfamethoxazole initiated at the outset of urinary tract infection and twice weekly is a valuable drug in children, provided the organism responsible for the infection is sensitive to this agent.  (+info)

Efficient protection of human bronchial epithelial cells against sulfur and nitrogen mustard cytotoxicity using drug combinations. (2/45)

The aim of this study was to test the efficacy of several candidate molecules against sulfur mustard (SM) and nitrogen mustard (HN2) using a human bronchial-epithelial cell line (16HBE14o-). Candidate molecules were chosen on the basis of the known cytotoxicity mechanisms of mustards or their efficacy previously observed on other cellular models. It included the sulfhydryl-containing molecules N-acetyl-cysteine (NAC) and WR-1065, the nucleophile hexamethylenetetramine (HMT), the energy-level stabilizer niacinamide (NC), the antioxidant dimethylthiourea (DMTU), L-arginine analogues such as L-thiocitrulline (L-TC) and L-nitroarginine methyl ester (L-NAME), and the anti-gelatinase doxycycline (DOX). Their efficacy was determined using 2-(4-[3-iodophenyl)-3-(4-nitrophenyl)-5-(2, 4-disulfophenyl)-2Htetrazolium (WST-1) reduction by viable cells 24 h after initial exposure to 100 microM HN2 or SM. On individual immediate cotreatment, some molecules exhibited selective protection against only one mustard, such as DMTU and WR-1065 against HN2 and DOX against SM, whereas NAC and L-TC were effective against both SM and HN2 cytotoxicity. However, as the level of protection against SM was always weak compared to HN2, several combinations were investigated against SM to improve the protection. The effective combinations (L-TC + DOX, NAC + DOX, NAC + DMTU, NAC + HMT, NC + DOX) combined agents, reducing the bioavailability of the mustard with compounds possibly acting on the consequences of alkylation. One of these combinations, NAC + DOX, appeared to be the most interesting, as these agents are already used in human therapy. It exhibited good efficacy in delayed cotreatment (up to 90 min) against SM.  (+info)

Application of fluorescent in situ hybridization for specific diagnosis of Pneumocystis carinii pneumonia in foals and pigs. (3/45)

Fluorescent in situ hybridization, immunohistochemistry, and Grocott's methenamine-silver nitrate staining were compared as diagnostic methods for Pneumocystis carinii pneumonia in formalin-fixed lung tissue from foals and pigs. An oligonucleotide probe targeting 18S ribosomal RNA of P. carinii was designed for in situ hybridization, and a commercially available monoclonal antibody was used for immunohistochemistry. Samples from six foals and 10 pigs with P. carinii pneumonia, as verified by Grocott's methenamine-silver nitrate staining, were examined concurrently with samples from seven animals with pneumonia caused by other pathogens. Fluorescent in situ hybridization showed distinctive positive reactions for P. carinii in all test samples. The immunohistochemical procedure, however, only revealed P. carinii in the foals. The number of P. carinii organisms observed by fluorescent in situ hybridization and immunohistochemistry far exceeded the number of organisms stained by Grocott's methenamine-silver nitrate staining. The results show that fluorescent in situ hybridization targeting ribosomal RNA can provide a specific diagnosis of P. carinii pneumonia in foals and pigs.  (+info)

Evaluation of lectin staining in the diagnosis of fungal keratitis in an experimental rabbit model. (4/45)

PURPOSE: To assess the sensitivity, specificity, and reliability of peroxidase labeled lectin staining in the diagnosis of fungal keratitis in an experimental rabbit model. METHODS: Fungal keratitis by Candida albicans, Aspergillus fumigatus, and Fusarium solani was induced in rabbits. WGA-peroxidase staining of 660 corneal sections was performed. Fungal staining was evaluated independently by two observers. The test sensitivity, specificity, and reliability indexes were calculated. RESULTS: The sensitivity of the lectin staining test for Candida albicans was 100% (95% CI: 93.51-100.00), and specificity was 100% (95% CI: 93.51-100.00). The sensitivity of the test for Aspergillus fumigatus was 96.36% (95% CI: 86.46-99.35), and specificity was 100% (95% CI: 93.51-100.00). The sensitivity of the test for Fusarium solani was 96.36% (95% CI: 86.46-99.35) and specificity was 96.15% (95% CI: 85.74-99.31). There was also a high degree of test-retest and inter-rater concordance for all three fungi tested. The test-retest k reliability indexes were 0.9455, 0.9636, and 0.8879, for Candida albicans, Aspergillus fumigatus, and Fusarium solani, respectively. The inter-rater k reliability indexes were 0.9636, 0.9818, and 0.9252, for Candida albicans, Aspergillus fumigatus, and Fusarium solani, respectively. CONCLUSIONS: WGA-peroxidase staining is a very sensitive, specific, and reliable test for the identification of fungi in an experimental rabbit model of fungal keratitis.  (+info)

Developmental changes in the fine structure and histochemical properties of mucous cells in the parotid gland of the infant Japanese macaque. (5/45)

Mucous cells have been known to occur in the terminal portions of the parotid gland in a few species of mammals during a limited period of their development. The aim of this study was to examine the occurrence and features of mucous cells in the parotid gland of the infant Japanese macaque. Light microscopy revealed that mucous cells in the macaque parotid gland were present in the terminal clusters and acini at postnatal day 15, were less prevalent at day 30, and continued to decrease in number over 3 months. Mucous cells were no longer recognized in the parotid gland in 6-month-old macaques. Electron microscopy showed that the mucous cells contained electron-lucent secretory granules and bipartite or tripartite secretory granules. By 3 months of age, there was a scarcity of mucous cells and a concomitant increase in transitional cells. These transitional cells were intermediate in structure between mucous and serous cells, and contained three types of granules: electron-lucent, bipartite or tripartite, and electron-dense. None of the cells showed apoptotic figures. Lectin histochemistry indicated that the mucous cells in the early postnatal period had sugar residues identical in nature to those seen in the granules from mature serous cells in the glands of 3-month-old macaques. Immunohistochemistry using an antibody against human alpha-amylase showed a weakly positive reactivity in the secretory granules of the mucous cells, starting from day 15. In the transitional cells, the electron-dense granules showed a stronger immunoreactivity than either the electron-lucent granules or the heterogeneously structured granules. These results suggest that the secretory granules of mucous cells have characteristics in common with those of serous cells, and that during the transitional period the mucous granules change from the initial electron-lucent to hetorogenous forms, finally becoming the electron-dense granules. The mucous cells in the parotid gland of the juvenile Japanese macaque are therefore suggested to be converted into serous cells.  (+info)

Comparison of staining methods and a nested PCR assay to detect Histoplasma capsulatum in tissue sections. (6/45)

To optimize diagnosis of histoplasmosis in tissue sections, 30 spleen specimens from mice, experimentally infected with Histoplasma capsulatum, were examined by H&E, Grocott stain, anti-bacille Calmette-Guerin antibody immunostain, Fungiqual A fluorochrome stain (Drs Reinehr and Rembold, Kandern, Germany), and a nested polymerase chain reaction (PCR) assay. Results were compared with the tissue burden determined by quantitative culture. By applying logistic regression, the nested PCR assay was the most sensitive method, but not significantly more sensitive than the Grocott stain. The 50% quantile to achieve a positive result was determined to be 3 colony-forming units per milligram of spleen tissue for the PCR assay, 11 for the Grocott stain, 27 for the fluorochrome stain, 190 for immunostaining, and 533 for the H&E stain. The Grocott and fluorochrome stains did not differ significantly in detecting fungal elements. The PCR assay unambiguously identified H. capsulatum in tissue sections.  (+info)

Polyamine structural effects on the induction and stabilization of liquid crystalline DNA: potential applications to DNA packaging, gene therapy and polyamine therapeutics. (7/45)

DNA undergoes condensation, conformational transitions, aggregation and resolubilization in the presence of polyamines, positively charged organic molecules present in all cells. Under carefully controlled environmental conditions, DNA can also transform to a liquid crystalline state in vitro. We undertook the present work to examine the ability of spermidine, N4-methylspermidine, spermine, N1-acetylspermine and a group of tetramine, pentamine and hexamine analogs of spermine to induce and stabilize liquid crystalline DNA. Liquid crystalline textures were identified under a polarizing microscope. In the absence of polyamines, calf thymus DNA assumed a diffused, planar cholesteric phase with entrapped bubbles when incubated on a glass slide at 37 degrees C. In the presence of spermidine and spermine, the characteristic fingerprint textures of the cholesteric phase, adopting a hexagonal order, were obtained. The helical pitch was 2.5 micro m. The final structures were dendrimeric and crystalline when DNA was treated with spermine homologs and bis(ethyl) derivatives. A cholesteric structure was observed when DNA was treated with a hexamine at 37 degrees C. This structure changed to a hexagonal dendrimer with fluidity on prolonged incubation. These data show a structural specificity effect of polyamines on liquid crystalline phase transitions of DNA and suggest a possible physiological function of natural polyamines.  (+info)

A simple method for the specific detection of Ren-1 renin. (8/45)

BACKGROUND: Ren-1 and Ren-2 renin are expressed in the kidneys of all mice and in the submandibular gland of several mouse strains. The present study determined the usefulness of modified periodic acid silver-methenamine (PAM) staining for the specific detection of Ren-1 renin. METHODS: Conventional paraffin sections were prepared from kidneys of ICR, BALB/cA, C57BL/6Cr, C3H/HeN, DBA/2Cr, angiotensin II type 1a receptor gene knockout (AT1aKO) mice, Wistar rats and a human, and submandibular glands of C57BL/6Cr and DBA/2Cr mice. Sections were analyzed for the presence of renin using PAM and immunohistochemistry. PAM reactions were terminated at generally or weakly intense (weak PAM staining; W-PAM). In addition, kidneys of DBA/2Cr mice were fixed using various fixatives (formalin, PFA, PLP, Zamboni's, Bouin's, or Carnoy's) and treated using identical procedures. RESULTS: Although PAM-positive reactions were observed in juxtaglomerular (JG) cells, W-PAM reactions were particularly specific for these cells. These findings were observed in all mouse strains. Immunohistochemistry using mirror sections suggested that a W-PAM-positive reaction detected renin. This hypothesis was confirmed by the results from AT1aKO mice. Briefly, W-PAM detected an expansion of renin-positive areas in AT1aKO mice. Rat and human kidneys and mouse submandibular glands were negative for W-PAM. Levels of JG cell detection by W-PAM were similar in samples fixed in formalin, PFA, PLP, or Zamboni's. CONCLUSIONS: The present findings show that W-PAM can identify Ren-1 renin, but not Ren-2, rat or human renin. The W-PAM method is useful for the specific detection of Ren-1 renin.  (+info)

Methenamine is a medication that is used as a urinary antiseptic. It's a chemical compound that, when ingested and enters the urine, releases formaldehyde, which helps to kill bacteria in the urinary tract. Methenamine is often combined with other medications, such as sodium phosphate or hydroxyzine, to make it more effective.

It's important to note that methenamine is not typically used as a first-line treatment for urinary tract infections (UTIs) and is usually reserved for preventing recurrent UTIs in people who are prone to them. Additionally, methenamine should be taken in adequate amounts and under the guidance of a healthcare professional, as excessive formaldehyde release can cause adverse effects.

Phenazopyridine is a medication that functions as a urinary analgesic, which means it helps to relieve pain, burning, and discomfort in the urinary tract. It works by numbing the lining of the urinary tract, reducing the sensation of pain upon urination. Phenazopyridine is typically available in oral form, and its use is generally limited to short-term treatment (up to 2 days) of symptoms associated with urinary tract infections.

It is important to note that phenazopyridine does not treat the underlying infection; it only helps alleviate the discomfort caused by the infection. Antibiotics are necessary to address the infection itself. Moreover, phenazopyridine can cause side effects such as headache, dizziness, and stomach upset. It may also stain urine, sweat, and tears a reddish-orange color, which is harmless but can be alarming if not anticipated. Always consult with a healthcare professional for appropriate medical advice and treatment.

"Pneumocystis" is a genus of fungi that are commonly found in the lungs of many mammals, including humans. The most well-known and studied species within this genus is "Pneumocystis jirovecii," which was previously known as "Pneumocystis carinii." This organism can cause a serious lung infection known as Pneumocystis pneumonia (PCP) in individuals with weakened immune systems, such as those with HIV/AIDS or who are undergoing immunosuppressive therapy.

It's worth noting that while "Pneumocystis" was once classified as a protozoan, it is now considered to be a fungus based on its genetic and biochemical characteristics.

"Pneumonia, Pneumocystis" is more commonly referred to as "Pneumocystis pneumonia (PCP)." It is a type of pneumonia caused by the microorganism Pneumocystis jirovecii. This organism was previously classified as a protozoan but is now considered a fungus.

PCP is an opportunistic infection, which means that it mainly affects people with weakened immune systems, such as those with HIV/AIDS, cancer, transplant recipients, or people taking immunosuppressive medications. The symptoms of PCP can include cough, shortness of breath, fever, and difficulty exercising. It is a serious infection that requires prompt medical treatment, typically with antibiotics.

It's important to note that PCP is not the same as pneumococcal pneumonia, which is caused by the bacterium Streptococcus pneumoniae. While both conditions are types of pneumonia, they are caused by different organisms and require different treatments.

'Staining and labeling' are techniques commonly used in pathology, histology, cytology, and molecular biology to highlight or identify specific components or structures within tissues, cells, or molecules. These methods enable researchers and medical professionals to visualize and analyze the distribution, localization, and interaction of biological entities, contributing to a better understanding of diseases, cellular processes, and potential therapeutic targets.

Medical definitions for 'staining' and 'labeling' are as follows:

1. Staining: A process that involves applying dyes or stains to tissues, cells, or molecules to enhance their contrast and reveal specific structures or components. Stains can be categorized into basic stains (which highlight acidic structures) and acidic stains (which highlight basic structures). Common staining techniques include Hematoxylin and Eosin (H&E), which differentiates cell nuclei from the surrounding cytoplasm and extracellular matrix; special stains, such as PAS (Periodic Acid-Schiff) for carbohydrates or Masson's trichrome for collagen fibers; and immunostains, which use antibodies to target specific proteins.
2. Labeling: A process that involves attaching a detectable marker or tag to a molecule of interest, allowing its identification, quantification, or tracking within a biological system. Labels can be direct, where the marker is directly conjugated to the targeting molecule, or indirect, where an intermediate linker molecule is used to attach the label to the target. Common labeling techniques include fluorescent labels (such as FITC, TRITC, or Alexa Fluor), enzymatic labels (such as horseradish peroxidase or alkaline phosphatase), and radioactive labels (such as ³²P or ¹⁴C). Labeling is often used in conjunction with staining techniques to enhance the specificity and sensitivity of detection.

Together, staining and labeling provide valuable tools for medical research, diagnostics, and therapeutic development, offering insights into cellular and molecular processes that underlie health and disease.

Cystitis is a medical term that refers to inflammation of the bladder, usually caused by a bacterial infection. The infection can occur when bacteria from the digestive tract or skin enter the urinary tract through the urethra and travel up to the bladder. This condition is more common in women than men due to their shorter urethras, which makes it easier for bacteria to reach the bladder.

Symptoms of cystitis may include a strong, frequent, or urgent need to urinate, pain or burning during urination, cloudy or strong-smelling urine, and discomfort in the lower abdomen or back. In some cases, there may be blood in the urine, fever, chills, or nausea and vomiting.

Cystitis can usually be treated with antibiotics to kill the bacteria causing the infection. Drinking plenty of water to flush out the bacteria and alleviating symptoms with over-the-counter pain medications may also help. Preventive measures include practicing good hygiene, wiping from front to back after using the toilet, urinating after sexual activity, and avoiding using douches or perfumes in the genital area.

Lower urinary tract symptoms (LUTS) refer to a group of clinical symptoms related to the lower urinary tract, including the bladder and urethra. These symptoms can be categorized into storage, voiding, and post-micturition symptoms. Storage symptoms include frequency, urgency, nocturia, and urinary incontinence. Voiding symptoms consist of hesitancy, slow stream, straining, and intermittent flow. Post-micturition symptoms include a feeling of incomplete bladder emptying and post-void dribbling. LUTS can be caused by various underlying conditions such as benign prostatic hyperplasia (BPH), overactive bladder (OAB), urinary tract infection, neurogenic bladder dysfunction, or bladder cancer. The evaluation and management of LUTS require a comprehensive assessment of the patient's medical history, physical examination, and appropriate diagnostic tests to determine the underlying cause and develop an effective treatment plan.

Hematuria is a medical term that refers to the presence of blood in urine. It can be visible to the naked eye, which is called gross hematuria, or detected only under a microscope, known as microscopic hematuria. The blood in urine may come from any site along the urinary tract, including the kidneys, ureters, bladder, or urethra. Hematuria can be a symptom of various medical conditions, such as urinary tract infections, kidney stones, kidney disease, or cancer of the urinary tract. It is essential to consult a healthcare professional if you notice blood in your urine to determine the underlying cause and receive appropriate treatment.

BK virus, also known as BK polyomavirus, is a type of virus that belongs to the Polyomaviridae family. It is named after the initials of a patient in whom the virus was first isolated. The BK virus is a common infection in humans and is typically acquired during childhood. After the initial infection, the virus remains dormant in the body, often found in the urinary tract and kidneys.

In immunocompetent individuals, the virus usually does not cause any significant problems. However, in people with weakened immune systems, such as those who have undergone organ transplantation or have HIV/AIDS, BK virus can lead to severe complications. One of the most common manifestations of BK virus infection in immunocompromised individuals is hemorrhagic cystitis, a condition characterized by inflammation and bleeding in the bladder. In transplant recipients, BK virus can also cause nephropathy, leading to kidney damage or even failure.

There is no specific treatment for BK virus infection, but antiviral medications may be used to help control the virus's replication in some cases. Maintaining a strong immune system and monitoring viral load through regular testing are essential strategies for managing BK virus infections in immunocompromised individuals.

Urination disorders, also known as lower urinary tract symptoms (LUTS), refer to a range of clinical conditions that affect the bladder and urethra, resulting in abnormalities in the storage, transportation, and evacuation of urine. These disorders can be categorized into voiding symptoms, such as hesitancy, straining, slow stream, intermittency, and terminal dribble; and storage symptoms, including frequency, urgency, nocturia, and urge incontinence.

The causes of urination disorders are diverse, encompassing congenital abnormalities, neurological conditions, infections, inflammation, medications, and age-related changes. Common underlying pathologies include bladder overactivity, detrusor muscle instability, underactive bladder, and obstruction of the urethra.

Urination disorders can significantly impact an individual's quality of life, causing physical discomfort, sleep disturbances, emotional distress, and social isolation. Accurate diagnosis and appropriate management require a comprehensive assessment of the patient's medical history, physical examination, urinalysis, and urodynamic studies. Treatment options may include behavioral modifications, pelvic floor exercises, bladder training, medications, neuromodulation, and surgical interventions.

The urinary bladder is a muscular, hollow organ in the pelvis that stores urine before it is released from the body. It expands as it fills with urine and contracts when emptying. The typical adult bladder can hold between 400 to 600 milliliters of urine for about 2-5 hours before the urge to urinate occurs. The wall of the bladder contains several layers, including a mucous membrane, a layer of smooth muscle (detrusor muscle), and an outer fibrous adventitia. The muscles of the bladder neck and urethra remain contracted to prevent leakage of urine during filling, and they relax during voiding to allow the urine to flow out through the urethra.

Hemorrhage is defined in the medical context as an excessive loss of blood from the circulatory system, which can occur due to various reasons such as injury, surgery, or underlying health conditions that affect blood clotting or the integrity of blood vessels. The bleeding may be internal, external, visible, or concealed, and it can vary in severity from minor to life-threatening, depending on the location and extent of the bleeding. Hemorrhage is a serious medical emergency that requires immediate attention and treatment to prevent further blood loss, organ damage, and potential death.

Methenamine Nassar A, Zapata M, Little JV, Siddiqui MT (November 2006). "Utility of reflex gomori methenamine silver staining ... In pathology, the Grocott-Gömöri's methenamine silver stain, abbreviated GMS, is a popular staining method in histology. The ... "Grocott-Gomori's Methenamine Silver Staining". Microbe Notes. 2021-02-08. Retrieved 2022-01-03. (Staining). ...
On microscopy, Aspergillus species are reliably demonstrated by silver stains, e.g., Gridley stain or Gomori methenamine-silver ... using Grocott's methenamine silver stain Angioinvasive pulmonary aspergillosis Angioinvasive pulmonary aspergillosis (closeup) ...
Methenamine compounds, reduces the urinary excretion of methenamines. Phenytoin, reduces phenytoin excretion, hence increasing ...
As methenamine is an antiseptic, it may avoid the issue of antibiotic resistance. Methenamine acts as an over-the-counter ... Methenamine silver stains are used for staining in histology, including the following types: Grocott's methenamine silver stain ... As the mandelic acid salt (methenamine mandelate) or the hippuric acid salt (methenamine hippurate), it is used for the ... Jones' stain, a methenamine silver-Periodic acid-Schiff that stains for basement membrane, availing to view the "spiked" ...
Methenamine in the form of cream or spray is effective in the treatment of excessive sweating and attendant odor. ... Methenamine (hexamethylenetetramine, also known as hexamine or urotropin) is a powerful antiperspirant, often used for severe ... Susak, Z.; Minkov, R.; Isakov, E. (1996). "The use of Methenamine as an antiperspirant for amputees". Prosthetics and Orthotics ...
Methenamine is another agent used for this purpose as in the bladder where the acidity is low it produces formaldehyde to which ... As methenamine is an antiseptic, it may avoid the issue of antibiotic resistance. In cases where infections are related to ... "Methenamine is as good as antibiotics at preventing urinary tract infections". NIHR Evidence. 20 December 2022. doi:10.3310/ ... A UK study showed that methenamine is as effective daily low-dose antibiotics at preventing UTIs among women who experience ...
He developed the Gömöri trichrome stain and Gömöri methenamine silver stain. Gömöri died at his home in Palo Alto, California, ...
Strom, J. Grady; Jun, H. Won (1993). "Effect of urine pH and ascorbic acid on the rate of conversion of methenamine to ... It is sometimes used as a urinary acidifier to enhance the antiseptic effect of methenamine. Natural biosynthesis of vitamin C ... "Effect of urinary acidifiers on formaldehyde concentration and efficacy with methenamine therapy". European Journal of Clinical ...
... , also Jones stain, is a methenamine silver-Periodic acid-Schiff stain used in pathology. It is also referred to as ... methenamine PAS which is commonly abbreviated MPAS. It stains for basement membrane and is widely used in the investigation of ...
Drugs that can decrease urine pH include ammonium chloride, chlorothiazide diuretics, and methenamine mandelate. Human urine ...
The fuel tablets are also known as hexamethyl-enetetramine, methenamine, "hexi tabs" or even simply "tabs". Hexi-stoves are ...
The "methenamine pill test" (ASTM D 2859) is used to judge the ignitability of flooring carpet. Flammability Fire test Fire- ...
Grocott's methenamine silver stain (GMS) will stain both living and dead fungal organisms. It is used to identify glycogen in ...
A Gomori methenamine silver stain can then confirm the presence of the Coccidioides organism's characteristic spherules within ...
There are several silver stains incorporating methenamine, including: Grocott's methenamine silver stain, used widely as a ... Jones' stain, a methenamine silver-Periodic acid-Schiff that stains for basement membrane, availing to view the "spiked" GBM ...
... such as periodic acid schiff and Gömöri methenamine silver, can be used to demonstrate the fungal organisms if needed.[citation ...
Newer methods include Gomori-Methenamine Silver staining and Perioidic Acid Schiff staining to color Mycobacterium avium ...
Identified by methenamine silver stain of lung tissue, type I pneumocytes, and type II pneumocytes over-replicate and damage ...
Histopathological study with Gomori methenamine silver (GMS) stain or hematoxylin and eosin (H&E) stain revealing large yeast ...
Tissue Gram or Grocott's methenamine silver stain. A radiological diagnosis may be helpful in elucidating the extent of the ...
... sputum and biopsy tissue by methods of Papanicolaou or Grocott's methenamine silver staining. These stains can demonstrate ...
... acid fast bacilli stain and Gömöri methenamine silver stain) to rule out microorganisms and fungi. Serum markers of sarcoidosis ...
The steam can be generated from a variety of sources, ranging from messy solid pellet (i.e. methenamine) or sterno-type fuel, ...
... vasopressor epinephrine MetroGel-Vaginal anti-infective metronidazole Urex urine tract anti-infective methenamine Minitran ...
Methenamine (INN) Metheptazine (INN) Methergine Methestrol (INN) Methiodal sodium (INN) Methiomeprazine (INN) Methionine (INN) ...
... after testing with Grocott's methenamine silver stain and Lactophenol cotton blue, confirmed the presence of dematiaceous ...
Gömöri methenamine silver stain (histology) Lewis Gompertz (c. 1783-1861), UK - expanding chuck, improved velocipede Sarah E. ...
... proprietary apps and services from Google bundled with Android devices Grocott's methenamine silver stain, histological stain ...
... methenamine MeSH D02.092.782.590 - pentetic acid MeSH D02.092.782.590.401 - gadolinium dtpa MeSH D02.092.782.590.883 - ... methenamine MeSH D02.455.426.100.050.750 - rimantadine MeSH D02.455.426.100.080 - bicyclo compounds MeSH D02.455.426.100. ...
... and land surface components Mornington Peninsula Astronomical Society Methenamine Periodic Acid Schiff Stain, or Jones' stain ...

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