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Journal of Autism and Developmental Disorders|August 10, 2006
Fragmented visuospatial processing in children with pervasive developmental disorderWim A J M Schlooz, Wouter Hulstijn, Pieter J A van den Broek, et al.
Neurology|May 5, 1999
Sjögren-Larsson syndrome: clinical and MRI/MRS findings in FALDH-deficient patientsP H van Domburg, M A Willemsen, J J Rotteveel, et al.
Orphanet Journal of Rare Diseases|September 11, 2022
Distress and post-traumatic stress in parents of patients with congenital gastrointestinal malformations: a cross-sectional cohort studyD Roorda, A F W van der Steeg, M van Dijk, et al.
Neuropediatrics|March 17, 2006
Clinical findings and a therapeutic trial in the first patient with beta-ureidopropionase deficiencyB Assmann, G Göhlich, M Baethmann, et al.
Neurology|August 2, 2008
Prognostic factors after a first attack of inflammatory CNS demyelination in childrenR F Neuteboom, M Boon, C E Catsman Berrevoets, et al.
Clinical Endocrinology|November 21, 2014
New insights into factors influencing adult height in short SGA children: Results of a large multicentre growth hormone trialJ S Renes, R H Willemsen, J C Mulder, et al.
Human Genetics|May 14, 2018
Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunctionMieke Wesdorp, Pia A M de Koning Gans, Margit Schraders, et al.
The Journal of Clinical Endocrinology and Metabolism|February 11, 2015
Bone mineral density in children and adolescents with Prader-Willi syndrome: a longitudinal study during puberty and 9 years of growth hormone treatmentN E Bakker, R J Kuppens, E P C Siemensma, et al.
The Journal of Clinical Endocrinology and Metabolism|September 5, 2013
Eight years of growth hormone treatment in children with Prader-Willi syndrome: maintaining the positive effectsN E Bakker, R J Kuppens, E P C Siemensma, et al.
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