Zobrazeno 1 - 10
of 28
pro vyhledávání: '"J M, Gertner"'
Autor:
M, Thearle, M, Horlick, J P, Bilezikian, J, Levy, J M, Gertner, L S, Levine, M, Harbison, W, Berdon, S E, Oberfield
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(6)
Osteoporosis is known to be associated with Crohn's disease. We report a 12-yr-old boy without a history of steroid use, in whom severe osteoporosis and multiple collapsed vertebrae were the presenting manifestations of Crohn's disease. After treatme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f097cfb7ff3e9c55698c95f1825facbb
https://pubmed.ncbi.nlm.nih.gov/10852438
https://pubmed.ncbi.nlm.nih.gov/10852438
Publikováno v:
Journal of acquired immune deficiency syndromes (1999). 21(4)
As part of the Hemophilia Growth and Development Study (HGDS), we investigated the relationship between HIV-associated immune dysfunction and delayed pubertal development in a cohort of 333 boys and adolescents with moderate or severe hemophilia who
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f824e1d13919fe793e7ea86e28e33e6
https://pubmed.ncbi.nlm.nih.gov/10428113
https://pubmed.ncbi.nlm.nih.gov/10428113
Autor:
P H, Dixon, P T, Christie, C, Wooding, D, Trump, M, Grieff, I, Holm, J M, Gertner, J, Schmidtke, B, Shah, N, Shaw, C, Smith, C, Tau, D, Schlessinger, M P, Whyte, R V, Thakker
Publikováno v:
The Journal of clinical endocrinology and metabolism. 83(10)
Hypophosphatemic rickets is commonly an X-linked dominant disorder (XLH or HYP) associated with a renal tubular defect in phosphate transport and bone deformities. The XLH gene, referred to as PHEX, or formerly as PEX (phosphate regulating gene with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::550279771c76db0c82ca48e9b7311740
https://pubmed.ncbi.nlm.nih.gov/9768674
https://pubmed.ncbi.nlm.nih.gov/9768674
Publikováno v:
The Journal of clinical endocrinology and metabolism. 83(7)
A role for GH in the pathogenesis of diabetic retinopathy has long been postulated. Previous clinical studies, however, have been confounded by hyperglycemia. We have identified 2 cases of retinopathy associated with exogenous GH therapy in nondiabet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::199ee52dd0b1e6fca2aac02436e14c21
https://pubmed.ncbi.nlm.nih.gov/10690911
https://pubmed.ncbi.nlm.nih.gov/10690911
Publikováno v:
Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association. 15(2)
Growth and pubertal development in hemophilic males, age 6-19 years at baseline, were evaluated over a 3.5-year period in 207 HIV-positive and 126 HIV-negative subjects as part of the Hemophilia Growth and Development Study.Thyroid function, insulin-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f7d62c95960fa9d4908ffbbbc841c1f1
https://pubmed.ncbi.nlm.nih.gov/9241113
https://pubmed.ncbi.nlm.nih.gov/9241113
Autor:
Chee-Wai Woon, L. I. Akhmadullina, N. P. Barker, N. Z. Sherman, Douglas E. Peterson, J. M. Gertner, I. Rodionova
Publikováno v:
Journal of Clinical Oncology. 26:9514-9514
9514 Background: Naturally occurring ITF is a peptide produced predominantly in the gastrointestinal tract, where it plays a key role in mucosal restitution. The purpose of the current Phase II study was to evaluate safety and efficacy of rhITF admin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef2dab708d7d775de819d399c0b92eb3
https://doi.org/10.1200/jco.2008.26.15_suppl.9514
https://doi.org/10.1200/jco.2008.26.15_suppl.9514
Publikováno v:
Scopus-Elsevier
Glucocorticoids inhibit the growth hormone (GH) response to a variety of stimuli, including GH-releasing hormone (GHRH) in vivo, but they increase GHRH-stimulated GH secretion when added, in vitro, to animal and human pituitary cells. This discrepanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40a975e5ba36dc7dec5435775bca3772
https://pubmed.ncbi.nlm.nih.gov/1979261
https://pubmed.ncbi.nlm.nih.gov/1979261
Autor:
J M, Gertner, L, Root
Publikováno v:
The Orthopedic clinics of North America. 21(1)
Osteogenesis imperfecta describes a group of heritable disorders characterized by excessive bony fragility and reduced skeletal mass. It is classified in terms of its clinical manifestations, but our understanding of the underlying genetic defects in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::25a2dc1a126fdbef539961fbd1490161
https://pubmed.ncbi.nlm.nih.gov/2296455
https://pubmed.ncbi.nlm.nih.gov/2296455
Publikováno v:
Calcified Tissue Research. 22:63-67
Infantile nephropathic cystinosis is a disease in which affected children present with the consequences of renal tubular dysfunction. Usually these children develop progressive renal impairment and die before the age of 10. Rickets is usually an earl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::159723dbdf2618ed468ce7456bb66d84
https://doi.org/10.1007/bf02064042
https://doi.org/10.1007/bf02064042
Publikováno v:
Archives of Disease in Childhood. 53:312-315
We describe a boy who presented at 4 years of age with radiological hyperparathyroidism, osteosclerosis, and necrosis of the femoral heads. Plasma biochemistry was normal but the parathyroid hormone (PTH) level was very high. He was deaf and had an u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cddc367b4a85d75a37991a9351116c4
https://doi.org/10.1136/adc.53.4.312
https://doi.org/10.1136/adc.53.4.312