TITLE

Mucoviscidosis

AUTHOR(S)
Gaisford, Wilfrid
PUB. DATE
April 1965
SOURCE
British Medical Journal;4/17/1965, Vol. 1 Issue 5441, p1054
SOURCE TYPE
Review
DOC. TYPE
Book Review
ABSTRACT
No abstract available.
ACCESSION #
64058456

 

Related Articles

  • mucoviscidosis.  // Taber's Cyclopedic Medical Dictionary (2009);2009, Issue 21, p1503 

    A definition of the term "mucoviscidosis," which pertains to cystic fibrosis, is presented.

  • Cystic Fibrosis.  // World Book Science Dataset;1/1/2009, p1 

    Cystic Fibrosis, also called CF and Mucoviscidosis, a hereditary disorder of the exocrine glands, especially those that produce sweat and mucus. .) It is characterized by excessive secretion of salt in the sweat and by production of abnormally thick mucus in the pancreas and lungs.

  • Organization helping people with mucoviscidosis ordered to register as "foreign agent". Interfax // Russia & FSU General News;4/25/2013, p1 

    MOSCOW. April 25 (Interfax) - The charity organization Assistance to People with Mucoviscidosis has been warned by the Istra city prosecutors that it is required to register with the Russian Justice Ministry as a foreign agent.

  • mucoviscidosis.  // Taber's Cyclopedic Medical Dictionary;2005, p1396 

    A definition of the medical term "mucoviscidosis" is presented, which means cystic fibrosis. The definition is from the "Taber's Cyclopedic Medical Dictionary," published by F.A. Davis Co.

  • TrudnoÅ›ci diagnostyczne zaburzeÅ„ elektrolitowych i kwasowo-zasadowych u 1.5-miesiÄ™cznego chÅ‚opca - opis przypadku. Kik, Eugenia; Noczyńska, Anna // Pediatric Endocrinology / Endokrynologia Pediatryczna;2014, Vol. 17 Issue 2, p85 

    The subject of the study is a 1.5 month old baby boy admitted to the clinic with hyponatremia and dehydration with suspected congenital adrenal hyperplasia. Laboratory findings showed hyponatremia, hypochloremia, hypokalemia, metabolic alkalosis. Congenital adrenal hyperplasia was excluded as a...

  • Chapter 10: Electroconductive textile electrodes for detection and analysis of sweat and urine. Westbroek, P.; Priniotakis, G.; Kiekens, P. // Analytical Electrochemistry in Textiles;2005, p274 

    The article presents a discussion regarding electroconductive textile electrodes for the detection and analysis of sweat and urine. It is comprised of five sections which include the introduction, description of the cell configuration, conditions for using yarn electrodes, cell configuration...

  • Warning Sweat.  // Time;8/5/1957, Vol. 70 Issue 6, p58 

    The article offers information on cystic fibrosis or mucoviscidosis, a condition wherein victims have a fibrous, diseased pancreas that does not secrete enough trypsin required in digestion. It states that cystic fibrosis affects glands throughout the body, and its symptoms include excessive...

  • Cystic fibrosis and Crohn's disease: Successful treatment and long term remission with infliximab. Vincenzi, Francesca; Bizzarri, Barbara; Ghiselli, Alessia; de' Angelis, Nicola; Fornaroli, Fabiola; de' Angelis, Gian Luigi // Annals of Gastroenterology & Hepatology;2010, Vol. 8 Issue 85, p1924 

    The association of cystic fibrosis and Crohn's disease (CD) is well known, but to date, there are very few cases in the literature of patients suffering from mucoviscidosis who have required treatment with infliximab. We report the case of a 23-year-old patient suffering from cystic fibrosis and...

  • Stigma and Cystic Fibrosis. Maues Peluci Pizzignacco, Tainá; de Mello, Débora Falleiros; de Lima, Regina Aparecida Garcia // Revista Latino-Americana de Enfermagem (RLAE);Jan/Feb2010, Vol. 18 Issue 1, p139 

    Cystic Fibrosis (CF), also known as Mucoviscidosis, is a chronic disease of autosomal recessive origin and so far incurable. This analysis considers some characteristics of patients and family members that indicate it is a stigmatizing disease. The CF stigma's impact on the lives of children and...

  • Algoritm de diagnostic în colestază la copil (I). Popovici, Paula; Moraru, Evelina // Pediatru.ro;2014, Issue 35, p6 

    Cystic fibrosis (mucoviscidosis) is the most common autosomal recessive disease in civilized countries in white population, with an incidence of 1 to 2500 live births. Multisystemic involvement is due to exocrine glands' dysfunction, particularly seen in respiratory and digestive diseases:...

Share

Read the Article

Courtesy of THE LIBRARY OF VIRGINIA

Sorry, but this item is not currently available from your library.

Try another library?
Sign out of this library

Other Topics