Search Results - "Romer, T E"

Effects of the Infusion of Insulin-like Growth Factor I in a Child with Growth Hormone Insensitivity Syndrome (Laron Dwarfism) by Walker, Jan L, Ginalska-Malinowska, Maria, Romer, Tomasz E, Pucilowska, Jolanta B, Underwood, Louis E

“…THE clinical manifestations of the growth hormone insensitivity syndrome (Laron dwarfism) result from the inability of growth hormone to exert its biologic…”
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The influence of prenatal dexamethasone treatment on urinary excretion of adrenocortical steroids in newborns by MAŁUNOWICZ, E. M, GINALSKA-MALINOWSKA, M, ROMER, T. E, BAL, K

“…Congenital adrenal hyperplasia due to 21-hydroxylase deficiency suspected in 14 newborns (5 F, 9 M), was treated prenatally with dexamethasone from weeks 7-9…”
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Growth hormone-releasing hormone reverses secondary somatotroph unresponsiveness by Romer, T E, Rymkiewicz-Kluczynska, B, Olivier, M, Sagnard, L, Szarras-Czapnik, M

“…Twenty severely GH-deficient prepubertal children aged 10.7 +/- 2.1 yr (mean +/- SD) and with a height SD of -4.92 +/- 1.02 were treated with sc injections of…”
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Definitive diagnosis of enzymatic deficiencies of steroidogenesis in at-risk newborns and infants by urinary marker analysis using GC/MS-SIM by Małunowicz, E M, Mitkowska, Z, Bal, K, Nizankowska-Błaz, T, Moszczyńska, E, Iwanicka, Z, Romer, T E

“…A simplified urinary marker analysis for diagnosis of congenital adrenal hyperplasia (CAH) and 5alpha-reductase deficiency in infancy by GC/MS-SIM is…”
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Luteinizing hormone secreting adrenal tumour as a cause of precocious puberty by Romer, Tomasz E., Sachnowska, Katrzyna, Savage, Martin O., Wozniewicz, Bogdan, Lowe, David G., Kula, Krzysztof K., Janas, Roman, Malendowicz, Ludwik, Besser, G. Michael

“…A boy aged 6 years presented with genital precocity, enlarged testes and advanced linear growth. An ovoid mass 3–4 cm in diameter was identified by MRI scan in…”
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Mutant luteinizing hormone receptors in a compound heterozygous patient with complete Leydig cell hypoplasia: abnormal processing causes signaling deficiency by Martens, J W M, Lumbroso, S, Verhoef-Post, M, Georget, V, Richter-Unruh, A, Szarras-Czapnik, M, Romer, T E, Brunner, H G, Themmen, A P N, Sultan, Ch

“…Over the past 5 yr several inactivating mutations in the LH receptor gene have been demonstrated to cause Leydig cell hypoplasia, a rare autosomal recessive…”
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Molecular study of the 5 alpha-reductase type 2 gene in three European families with 5 alpha-reductase deficiency by Boudon, C, Lumbroso, S, Lobaccaro, J M, Szarras-Czapnik, M, Romer, T E, Garandeau, P, Montoya, P, Sultan, C

“…The molecular basis of 5 alpha-reductase (5 alpha R) deficiency was investigated in four patients from three European families. In the French family, the first…”
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Oral clonidine for screening of growth hormone deficiency by Romer, T E, Rymkiewicz-Kluczynska, B, Bogoniowska, Z

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Somatic and germinal cells' interrelationship in the course of seminiferous tubule maturation in man by Kula, K, Romer, T E, Wlodarczyk, W P

“…Certain successive phases of seminiferous tubule maturation were observed in a transsection of a Leydig cell adenoma-bearing testis of a boy with precocious…”
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CORTICOSTEROIDS IN BROWN FAT BY A HISTOCHEMICAL METHOD by ROMER, TOMASZ E.

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Heterogeneity of urinary steroid profiles in children with adrenocortical tumors by Małunowicz, E M, Ginalska-Malinowska, M, Romer, T E, Ruszczyńska-Wolska, A, Dura, M

“…The excretory patterns of urinary steroids determined by capillary gas chromatography in 11 children (aged 0.8-16.5 years) with adrenocortical tumors were…”
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A case of Cushing's disease with growth retardation as its sole feature by Lastowiecki, P, Romer, T E

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Successful prenatal treatment of congenital adrenal hyperplasia resulting from the 21-hydroxylase deficiency: is prenatal diagnosis in a mother at risk essential? by Romer, T E, Ginalska-Malinowska, M

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Mutant Luteinizing Hormone Receptors in a Compound Heterozygous Patient with Complete Leydig Cell Hypoplasia: Abnormal Processing Causes Signaling Deficiency by Martens, J. W. M., Lumbroso, S., Verhoef-Post, M., Georget, V., Richter-Unruh, A., Szarras-Czapnik, M., Romer, T. E., Brunner, H. G., Themmen, A. P. N., Sultan, C.

“…Over the past 5 yr several inactivating mutations in the LH receptor gene have been demonstrated to cause Leydig cell hypoplasia, a rare autosomal recessive…”
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Nonspecific esterases in sex chromatin negative and positive cells in buccal smears by Romer, T E

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Use of bromocriptine for treatment of Cushing's disease caused by an adenoma originating from the intermediate lobe of the pituitary by Romer, T E, Lastowiecki, P M, Klimaszewski, J

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Body proportions in children with precocious puberty by Pyzuk, M, Matera, M, Romer, T E

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The syndrome of adrenocortical unresponsiveness to ACTH with achalasia by Chrzanowska, B, Romer, T E, Baka-Jakubiak, M, Kansy, J

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The influence of anabolic drugs on sex chromatin in buccal cells by Romer, T E

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Somatocrinin--growth hormone releasing factor--another hypothalamic hormone for clinical use by Romer, T E, Rymkiewicz-Kluczyńska, B, Szarras-Czapnik, M

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