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The American Journal of the Medical Sciences|April 18, 2000
Rapid communication: the human FEM1B gene maps to chromosome 15q22 and is excluded as the gene for Bardet-Biedl syndrome, type 4T Ventura-Holman, N B Haider, J F MaherHuman Molecular Genetics|August 7, 2001
Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 miceN B Haider, J K Naggert, P M NishinaCureus|August 4, 2022
Anti-N-Methyl-D-Aspartate Receptor Encephalitis Complicated by Autoimmune Enteropathy and Pulmonary Embolism: A Rare CaseMaryam B Haider, Noren Din, Sophia Dar, et al.The Journal of Clinical Investigation|March 1, 1971
Influence of scar on left ventricular performance at the onset of myocardial ischemia: shock versus heart failureT J Regan, A J Passannante, M I Khan, et al.Journal of Experimental Neuroscience|May 12, 2016
Role of Nuclear Receptors in Central Nervous System Development and Associated DiseasesAna Maria Olivares, Oscar Andrés Moreno-Ramos, Neena B HaiderThe Journal of Laboratory and Clinical Medicine|January 1, 1989
Effects of diabetes on myocardial perfusion in the atherosclerotic monkeyB Haider, M Lyons, R Torres, et al.Human Molecular Genetics|May 17, 2002
Genetic modifiers of vision and hearingNeena B Haider, Akihiro Ikeda, Jürgen K Naggert, et al.Cureus|September 16, 2021
Subhepatic Abscess Unmasking the Silent Gastric and Pulmonary SarcoidosisBrinda Basida, Maryam B Haider, Anusha Bapatla, et al.European Journal of Gastroenterology & Hepatology|June 4, 2014
Practical treatment of Helicobacter pylori: a balanced view in changing timesSinéad M Smith, Rana B Haider, Humphrey O'Connor, et al.American Journal of Human Genetics|October 30, 1998
A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mappingN B Haider, R Carmi, H Shalev, et al.Pageof 14