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Archives of Disease in Childhood. Fetal and Neonatal Edition|May 1, 1995
Absence of acidosis in the initial presentation of propionic acidaemiaJ H Walter, J E Wraith, M A ClearyThe Journal of Foot Surgery|July 1, 1989
Use of the cannulated bone screw in rearfoot surgeryW A Chieppa, K H Sydnor, J H WalterNeuroreport|February 24, 2001
Disappearance of beta2-adrenergic receptors on astrocytes in canine distemper encephalitis: possible implications for the pathogenesis of multiple sclerosisJ De Keyser, N Wilczak, J H Walter, et al.Archives of Disease in Childhood|January 25, 2005
Maternal phenylketonuria: report from the United Kingdom Registry 1978-97P J Lee, D Ridout, J H Walter, et al.European Journal of Pediatrics|October 1, 1993
Biochemical control, genetic analysis and magnetic resonance imaging in patients with phenylketonuriaJ H Walter, L A Tyfield, J B Holton, et al.Metabolism: Clinical and Experimental|August 1, 1990
In vivo enzyme activity in inborn errors of metabolismG N Thompson, J H Walter, J V Leonard, et al.Australian Dental Journal|December 1, 1995
Temporomandibular disorders. 2. Non-surgical treatmentG Dimitroulis, H A Gremillion, M F Dolwick, et al.Pediatric Research|December 1, 1994
Phenylalanine kinetics in sick preterm neonates with respiratory distress syndromeG J Shortland, J H Walter, P J Fleming, et al.Journal of Inherited Metabolic Disease|September 1, 2004
The benefits of liver transplantation in glycogenosis type IbN Bhattacharya, N Heaton, M Rela, et al.Clinical Dysmorphology|May 11, 2002
Facial appearance in glycogen storage disease type IIIM A Cleary, J H Walter, B A Kerr, et al.Pageof 8