Some effects of handling techniques on returns of tagged Australian salmon, Arripis trutta (Bloch and Schneider)STANLEY, C. A.Australian journal of marine and freshwater research. 1983, Vol 34, Num 6, pp 845-855, issn 0067-1940Article

Suppression of insulin oversecretion by subcutaneous recombinant human insulin-like growth factor I in children with congenital hyperinsulinism due to defective β-cell sulfonylurea receptorKATZ, L. E. L; FERRY, R. J; STANLEY, C. A et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 9, pp 3117-3124, issn 0021-972XArticle

Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase geneSTANLEY, C. A; LIEU, Y. K; HSU, B. Y. L et al.The New England journal of medicine. 1998, Vol 338, Num 19, pp 1352-1357, issn 0028-4793Article

Hyperinsulinism in infants and childrenSTANLEY, C. A.The Pediatric clinics of North America. 1997, Vol 44, Num 2, pp 363-374, issn 0031-3955Article

Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporterBENNETT, M. J; HALE, D. E; POLLITT, R. J et al.Clinical cardiology (Mahwah, NJ). 1996, Vol 19, Num 3, pp 243-246, issn 0160-9289Article

Renal handling of carnitine in secondary carnitine deficiency disordersSTANLEY, C. A; BERRY, G. T; BENNETT, M. J et al.Pediatric research. 1993, Vol 34, Num 1, pp 89-97, issn 0031-3998Article

The personal experience of juvenile Huntington's disease : an interpretative phenomenological analysis of parents' accounts of the primary features of a rare genetic conditionSMITH, J. A; BREWER, H. M; EATOUGH, V et al.Clinical genetics. 2006, Vol 69, Num 6, pp 486-496, issn 0009-9163, 11 p.Article

Familial hyperinsulinism caused by an activating glucokinase mutationGLASER, B; KESAVAN, P; HEROLD, K. C et al.The New England journal of medicine. 1998, Vol 338, Num 4, pp 226-230, issn 0028-4793Article

Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal death : Postmortem diagnosis, prenatal exclusion in subsequent pregnancies, and biochemical specificity of the mitochondrial translocaseCHALMERS, R. A; STANLEY, C. A; ENGLISH, N et al.The Journal of pediatrics. 1997, Vol 131, Num 2, pp 220-225, issn 0022-3476Article

Sudden neonatal death in carnitine transporter deficiencyRINALDO, P; STANLEY, C. A; HSU, B. Y. L et al.The Journal of pediatrics. 1997, Vol 131, Num 2, pp 304-305, issn 0022-3476Article

Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyTREEM, W. R; SHOUP, M. E; HALE, D. E et al.The American journal of gastroenterology. 1996, Vol 91, Num 11, pp 2293-2300, issn 0002-9270Article

Interferon-γ corrects the respiratory burst defect in vitro in monocyte-derived macrophages from glycogen storage disease type 1b patientsMCCAWLEY, L. J; KORCHAK, M; CUTILLI, J. R et al.Pediatric research. 1993, Vol 34, Num 3, pp 265-269, issn 0031-3998Article

Massive hepatomegaly, steatosis, and secondary plasma carnitine deficiency in an infant with cystic fibrosisTREEM, W. R; STANLEY, C. A.Pediatrics (Evanston). 1989, Vol 83, Num 6, pp 993-997, issn 0031-4005Article

Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemiaHALE, D. E; BATSHAW, M. L; COATES, P. M et al.Pediatric research. 1985, Vol 19, Num 7, pp 666-671, issn 0031-3998Article

Metabolism: the effect of early feeding on plasma glucose levels in SGA infantsWRIGHT, L. L; STANLEY, C. A; ANDAY, E. K et al.Clinical pediatrics. 1983, Vol 22, Num 8, pp 539-541, issn 0009-9228Article

Multiple Phenotypes in Phosphoglucomutase 1 DeficiencyTEGTMEYER, L. C; RUST, S; HUIJBEN, K et al.The New England journal of medicine. 2014, Vol 370, Num 6, pp 533-542, issn 0028-4793, 10 p.Article

Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor geneGLASER, B; RYAN, F; DONATH, M et al.Diabetes (New York, NY). 1999, Vol 48, Num 8, pp 1652-1657, issn 0012-1797Article

Linkage-disequilibrium mapping without genotypingCHEUNG, V. G; GREGG, J. P; NELSON, S. F et al.Nature genetics. 1998, Vol 18, Num 3, pp 225-230, issn 1061-4036Article

A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinismNESTOROWICZ, A; INAGAKI, N; PERMUTT, M. A et al.Diabetes (New York, NY). 1997, Vol 46, Num 11, pp 1743-1748, issn 0012-1797Article

First prenatal diagnosis of the carnitine transporter defectCHRISTODOULOU, J; SIAK HONG TEO; HAMMOND, J et al.American journal of medical genetics. 1996, Vol 66, Num 1, pp 21-24, issn 0148-7299Article

Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyTREEM, W. R; RINALDO, P; HALE, D. E et al.Hepatology (Baltimore, Md.). 1994, Vol 19, Num 2, pp 339-345, issn 0270-9139Article

In vitro and in vivo effects of granulocyte colony-stimulating factor on neutrophils in glycogen storage disease type 1B : granulocyte colony-stimulating factor therapy corrects the neutropenia and the defects in respiratory burst activity and Ca²⁺ mobilizationMCCAWLEY, L. J; KORCHAK, H. M; DOUGLAS, S. D et al.Pediatric research. 1994, Vol 35, Num 1, pp 84-90, issn 0031-3998Article

Elevated plasma carnitine in the hepatic form of carnitine palmitoyltransferase-1 deficiencySTANLEY, C. A; SUNARYO, F; HALE, D. E et al.Journal of inherited metabolic disease. 1992, Vol 15, Num 5, pp 785-789, issn 0141-8955Article

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptakeSTANLEY, C. A; DELEEUW, S; WAPPNER, R. S et al.Annals of neurology. 1991, Vol 30, Num 5, pp 709-716, issn 0364-5134Article

Clinical management considerations in uncommon midline central nervous system anomaliesVANDYKE, D. C; QUINN, G. E; BRUCE, D. A et al.Dysmorphology and clinical genetics. 1987, Vol 1, Num 1, pp 6-11Article