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Research Square|March 30, 2023
Top Caregiver Concerns in Rett syndrome and related disorders: data from the US Natural History StudyJeffrey Lorenz Neul, Timothy A Benke, Eric D Marsh, et al.
Meditsinskaia Parazitologiia I Parazitarnye Bolezni|September 1, 1990
[The isoenzyme identification and pathogenic characteristics of the Leishmania isolated in natural foci of cutaneous leishmaniasis in the USSR]M V Strelkova, A V Shurkhal, L N Eliseev, et al.
Anti-Cancer Drugs|November 18, 2000
Glutathione S-transferase genetic polymorphisms and individual sensitivity to the ototoxic effect of cisplatinU Peters, S Preisler-Adams, A Hebeisen, et al.
Orphanet Journal of Rare Diseases|October 24, 2019
A placebo-controlled trial of folic acid and betaine in identical twins with Angelman syndromeJulia Han, Terry Jo Bichell, Stephanie Golden, et al.
Autism Research : Official Journal of the International Society for Autism Research|November 22, 2012
The behavioral phenotype in MECP2 duplication syndrome: a comparison with idiopathic autismSarika U Peters, Rachel J Hundley, Amy K Wilson, et al.
Annals of Neurology|May 31, 2020
Comparison of Core Features in Four Developmental Encephalopathies in the Rett Natural History StudyClare Cutri-French, Dallas Armstrong, Joni Saby, et al.
Nature Genetics|May 27, 2008
Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA clusterTrilochan Sahoo, Daniela del Gaudio, Jennifer R German, et al.
Contemporary Clinical Trials|February 12, 2022
Design and outcome measures of LAVENDER, a phase 3 study of trofinetide for Rett syndromeJeffrey L Neul, Alan K Percy, Timothy A Benke, et al.
European Journal of Human Genetics : EJHG|May 25, 2007
Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlationsTrilochan Sahoo, Carlos A Bacino, Jennifer R German, et al.
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