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Showing articles 0 to 9 of 9 Filter Applied: failure to thrive (Click to remove) Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998 Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss Neurol 90:e625-e631, Set, K.K.,et al, 2018 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease Neurol 77:1287-1294, Prust, M.,et al, 2011 Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996 MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991 Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification NEJM 313:139-181, Sly,W.S.,et al, 1985 Showing articles 0 to 9 of 9