Showing results (181-190 of 1,193) with videos related to
Sort By:
Pageof 120
Digestive Diseases and Sciences|November 21, 1998
Lactose malabsorption is associated with early signs of mental depression in females: a preliminary reportM Ledochowski, B Sperner-Unterweger, D FuchsBiochemical Pharmacology|March 21, 1997
Chronic immune stimulation, oxidative stress, and apoptosis in HIV infectionG Baier-Bitterlich, D Fuchs, H WachterDeutsche Medizinische Wochenschrift (1946)|August 21, 1981
[Ultrasound misdiagnosis of gallbladder concrements in "phrygian cap" deformity (author's transl)]E Gmelin, H Freitag, H D FuchsJournal of Acquired Immune Deficiency Syndromes and Human Retrovirology : Official Publication of the International Retrovirology Association|October 1, 1996
Role of neopterin and 7,8-dihydroneopterin in human immunodeficiency virus infection: marker for disease progression and pathogenic linkG Baier-Bitterlich, H Wachter, D FuchsImmunobiology|January 1, 1996
7,8-Dihydroneopterin upregulates interferon-gamma promoter in T cellsG Baier-Bitterlich, D Fuchs, H WachterClinical Genetics|March 22, 2001
Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocationJ Seidel, S Schiller, C Kelbova, et al.Proceedings of the National Academy of Sciences of the United States of America|April 26, 2001
IL-4 determines eicosanoid formation in dendritic cells by down-regulation of 5-lipoxygenase and up-regulation of 15-lipoxygenase 1 expressionR Spanbroek, M Hildner, A Köhler, et al.European Journal of Haematology|November 28, 2001
Periodic fever (TRAPS) caused by mutations in the TNFalpha receptor 1 (TNFRSF1A) gene of three German patientsA Rösen-Wolff, H W Kreth, S Hofmann, et al.Journal of Learning Disabilities|August 1, 1994
Effects of classwide curriculum-based measurement and peer tutoring: a collaborative researcher-practitioner interview studyN B Phillips, L S Fuchs, D FuchsCellular and Molecular Biology (Noisy-Le-Grand, France)|April 9, 2002
Disturbed copper transport in humans. Part 1: mutations of the ATP7A gene lead to Menkes disease and occipital horn syndromeJ Seidel, L B Møller, H J Mentzel, et al.Pageof 120