Search Results - "Hopwood, Nancy"

Hyperinsulinism and Hyperammonemia in Infants with Regulatory Mutations of the Glutamate Dehydrogenase Gene by Stanley, Charles A, Lieu, Yen K, Hsu, Betty Y.L, Burlina, Alberto B, Greenberg, Cheryl R, Hopwood, Nancy J, Perlman, Kusiel, Rich, Barry H, Zammarchi, Enrico, Poncz, Mortimer

“…Congenital hyperinsulinism is the most common cause of recurrent hypoglycemia in early infancy. 1 Affected children present with seizures or coma and are at…”
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Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3 by Solomon, Nicola M, Ross, Shelley A, Forrest, Susan M, Thomas, Paul Q, Morgan, Thomas, Belsky, Joseph L, Hol, Frans A, Karnes, Pamela S, Hopwood, Nancy J, Myers, Susan E, Tan, Anjanette S, Warne, Garry L

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Treatment of the infant with congenital hypothyroidism by Hopwood, Nancy J.

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Diagnostic Quandary: Premature Ovarian Failure and Galactosemia Variants in Adolescent Girls with Delayed Puberty by Flint, Amanda C., MD, Hopwood, Nancy J., MD, Kasa-Vubu, Josephine Z., MD, MS

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Management quandary. Diagnostic quandary: premature ovarian failure and galactosemia variants in adolescent girls with delayed puberty by Flint, Amanda C, Hopwood, Nancy J, Kasa-Vubu, Josephine Z

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Partial growth-hormone insensitivity: The role of growth-hormone receptor mutations in idiopathic short stature by Goddard, Audrey D., Dowd, Patrick, Chernausek, Steven, Geffner, Mitchell, Gertner, Joseph, Hintz, Raymond, Hopwood, Nancy, Kaplan, Selna, Plotnick, Leslie, Rogol, Alan, Rosenfield, Robert, Saenger, Paul, Mauras, Nellie, Hershkopf, Richard, Angulo, Morris, Attie, Kenneth

“…Mutations in the GHR locus may play a role in the cause of idiopathic short stature (ISS) by impairing growth-hormone (GH) receptor (GHR) function. At one…”
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Thyroid masses: approach to diagnosis and management in childhood and adolescence by Hopwood, N J, Kelch, R P

“…The approach to the evaluation of a neck mass requires careful history and physical examination to determine if the mass is thyroidal or non-thyroidal…”
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High dose recombinant human growth hormone (GH) treatment of GH-deficient patients in puberty increases near-final height : A randomized, multicenter trial by MAURAS, Nelly, ATTIE, Kenneth M, REITER, Edward O, SAENGER, Paul, BAPTISTA, Joyce

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The Hormonal Phenotype of Nonclassic 3β-Hydroxysteroid Dehydrogenase (HSD3B) Deficiency in Hyperandrogenic Females Is Associated with Insulin-Resistant Polycystic Ovary Syndrome and Is Not a Variant of Inherited HSD3B2 Deficiency by Carbunaru, Goldy, Prasad, Pallavi, Scoccia, Bert, Shea, Patrick, Hopwood, Nancy, Ziai, Fuad, Chang, Ying Tai, Myers, Susan E., Mason, J. Ian, Pang, Songya

“…To test our hypothesis that the hormonal phenotype of mild 3β-hydroxysteroid dehydrogenase (HSD3B) deficiency in hyperandrogenic females (HF) is related to…”
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Nocturnal serum growth hormone concentration is not augmented by short-term testosterone infusion in pubertal boys by FOSTER, C. M, HOPWOOD, N. J, HASSING, J. M, HALE, P. M, MENDES, T, KELCH, R. P, BEITINS, I. Z

“…Chronic exposure to testosterone (T) increases growth hormone (GH) secretion. To determine whether acute exposure to T would also enhance GH secretion, we…”
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Evidence for decreased secretion of gonadotropin-releasing hormone in pubertal boys during short-term testosterone treatment by KELCH, R. P, HOPWOOD, N. J, SAUDER, S, MARSHALL, J. C

“…Information about the site(s) of action as well as the age-dependent effects of sex steroids on gonadotropin-releasing hormone and gonadotropin secretion…”
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Thick lips, bumpy tongue, and slipped capital femoral epiphysis--a deadly combination by Saltzman, C L, Herzenberg, J E, Phillips, W A, Hensinger, R N, Hopwood, N J

“…Multiple endocrine neoplasia type 2b (MEN 2b) is a rare genetic disorder. Affected individuals have malignant thyroid tumors, pheochromocytoma, and…”
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Psychosocial dwarfism: identification, intervention and planning by Bowden, M L, Hopwood, N J

“…Psychosocial Dwarfism, a syndrome caused by deprivation, emotional stress and/or neglect, occurs in both infants and children. The identification of children…”
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Growth hormone suppression of pancreatic polypeptide secretion by Zipf, W B, Kelch, R P, Floyd, J C, Hopwood, N J

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Incidence of Nelson's syndrome after adrenalectomy for Cushing's disease in children: results of a nationwide survey by Hopwood, N J, Kenny, F M

“…To establish the incidence of Nelson's syndrome in children treated with total bilateral adrenalectomy (TBA) for Cushing's disease, a survey was made of…”
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Growth response of children with non-growth-hormone deficiency and marked short stature during three years of growth hormone therapy by Hopwood, N J, Hintz, R L, Gertner, J M, Attie, K M, Johanson, A J, Baptista, J, Kuntze, J, Blizzard, R M, Cara, J F, Chernausek, S D

“…Short-term administration of human growth hormone to children with idiopathic short stature can improve mean growth rate and predicted adult height. It is yet…”
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Emotional deprivation. Report of a case with features of leprechaunism by Hopwood, N J, Powell, G F

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Familial precocious puberty in a brother and sister by Hopwood, N J, Kelch, R P, Helder, L J

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Fructose-1,6-diphosphatase deficiency by Hopwood, N J, Holzman, I, Drash, A L

“…A girl aged 3 years and 11 months, with recurrent episodes of unexplained metabolic acidosis, hepatomegaly, and fasting hypoglycemia unresponsive to glucagon,…”
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Hypoglycemia in hypopituitary children by Hopwood, N J, Forsman, P J, Kenny, F M, Drash, A L

“…Fifty-two children with growth hormone (GH) deficiency were examined for factors that might influence development of hypoglycemia. Symptomatic and asymptomatic…”
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