Authors:
ELLAWAY C
NORTH K
ARBUCKLE S
CHRISTODOULOU J
Citation: C. Ellaway et al., COMPLEX-I DEFICIENCY IN ASSOCIATION WITH STRUCTURAL ABNORMALITIES OF THE DIAPHRAGM AND BRAIN, Journal of inherited metabolic disease, 21(1), 1998, pp. 72-73
Authors:
FRAWLEY KJ
COHEN R
OLOUGHLIN EV
NORTH K
ARBUCKLE S
Citation: Kj. Frawley et al., NEUROFIBROMATOSIS OF THE SMALL-INTESTINE MESENTERY IN A CHILD WITH NEUROFIBROMATOSIS TYPE-1, Journal of pediatric surgery, 32(12), 1997, pp. 1783-1785
Citation: I. Datskou et K. North, RISKS DUE TO GROUNDWATER CONTAMINATION AT A PLUTONIUM PROCESSING FACILITY, Water, air and soil pollution, 90(1-2), 1996, pp. 133-141
Authors:
NORTH K
KORSON MS
KRAWIECKI N
SHOFFNER JM
HOLM IA
Citation: K. North et al., OXIDATIVE-PHOSPHORYLATION DEFECT ASSOCIATED WITH PRIMARY ADRENAL INSUFFICIENCY, The Journal of pediatrics, 128(5), 1996, pp. 688-692
Authors:
CIULLA TA
NORTH K
MCCABE O
ANTHONY DC
KORSON MS
PETERSEN RA
Citation: Ta. Ciulla et al., BILATERAL INFANTILE CATARACTOGENESIS IN A PATIENT WITH DEFICIENCY OF COMPLEX-I, A MITOCHONDRIAL ELECTRON-TRANSPORT CHAIN ENZYME, Journal of pediatric ophthalmology and strabismus, 32(6), 1995, pp. 378-382
Authors:
ASAMOAH A
NORTH K
DORAN S
WAGSTAFF J
OGLE R
COLLINS FS
KORF BR
Citation: A. Asamoah et al., 17Q INVERSION INVOLVING THE NEUROFIBROMATOSIS TYPE ONE LOCUS IN A FAMILY WITH NEUROFIBROMATOSIS TYPE ONE, American journal of medical genetics, 60(4), 1995, pp. 312-316
Authors:
NORTH K
JOY P
YUILLE D
COCKS N
HUTCHINS P
Citation: K. North et al., COGNITIVE FUNCTION AND ACADEMIC-PERFORMANCE IN CHILDREN WITH NEUROFIBROMATOSIS TYPE-1, Developmental Medicine and Child Neurology, 37(5), 1995, pp. 427-436
Citation: P. Joy et al., NEUROPSYCHOLOGICAL FUNCTION AND MRI ABNORMALITIES IN NEUROFIBROMATOSIS TYPE-1, Developmental Medicine and Child Neurology, 37(10), 1995, pp. 906-914
Authors:
KORSON M
NORTH K
HOPPEL C
DEGIROLAMI U
KOZAKEWICH H
Citation: M. Korson et al., LETHAL NEONATAL DEFICIENCY OF CARNITINE PALMITOYLTRANSFERASE-II ASSOCIATED WITH DYSGENESIS OF THE BRAIN AND KIDNEYS - A METABOLIC MALFORMATION SYNDROME WITH IMPLICATIONS FOR THE PATHOGENESIS OF ZELLWEGER-SYNDROME AND GLUTARIC ACIDEMIA TYPE-II, American journal of human genetics, 57(4), 1995, pp. 1034-1034
Authors:
NORTH K
JOY P
YUILLE D
COCKS N
MOBBS E
HUTCHINS P
MCHUGH K
DESILVA M
Citation: K. North et al., SPECIFIC LEARNING-DISABILITY IN CHILDREN WITH NEUROFIBROMATOSIS TYPE-1 - SIGNIFICANCE OF MRI ABNORMALITIES, Neurology, 44(5), 1994, pp. 878-883
Citation: K. North, NEUROFIBROMATOSIS TYPE-1 - REVIEW OF THE 1ST 200 PATIENTS IN AN AUSTRALIAN CLINIC, Journal of child neurology, 8(4), 1993, pp. 395-402
Citation: A. Asamoah et al., A 17Q INVERSION INVOLVING THE NF1 LOCUS IN A FAMILY WITH NEUROFIBROMATOSIS TYPE-1, American journal of human genetics, 53(3), 1993, pp. 1121-1121