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Alimentary Pharmacology & Therapeutics|September 9, 2004
Review article: exploration of the genetic aetiology of inflammatory bowel disease--implications for diagnosis and therapyS Schreiber, J Hanpe, S Nikolaus, et al.
Gastroenterology|May 1, 1995
Immunoregulatory role of interleukin 10 in patients with inflammatory bowel diseaseS Schreiber, T Heinig, H G Thiele, et al.
Biochemical Medicine and Metabolic Biology|October 1, 1986
The salivary flow rate and composition of whole and parotid resting and stimulated saliva in young and old healthy subjectsH Ben-Aryeh, A Shalev, R Szargel, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
A new autosomal recessive syndrome characterized by ocular hypertelorism, distinctive face, mental retardation, brachydactyly, and genital abnormalitiesRonen Spiegel, Yoseph Horovitz, Hartmut Peters, et al.
Genetic Testing|March 21, 2006
High incidence of deafness from three frequent connexin 26 mutations in an isolated communityJoël Zlotogora, Minerva Carasquillo, Saleh Barges, et al.
Pediatric Neurology|December 2, 2006
Hereditary hypotonia, muscle weakness, failure to thrive, and cognitive delay in a large moslem kindredMiriam Kutai, Stavit A Shalev, Ilana Chervinski, et al.
International Archives of Allergy and Immunology|February 8, 2007
A novel missense mutation in CIAS1 encoding the pyrin-like protein, cryopyrin, causes familial cold autoinflammatory syndrome in a family of Ethiopian originStavit A Shalev, Eli Sprecher, Margarita Indelman, et al.
Physiology & Behavior|October 23, 1997
Flunarizine analgesia is mediated by mu-opioid receptorsR Weizman, I A Pankova, S Schreiber, et al.
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