Zobrazeno 1 - 10
of 38
pro vyhledávání: '"C A, Sklar"'
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of alleles, including common alleles of small effect that might be detected by genome-wide association studies. Here we report a multi-stage schizophrenia genom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::6faaa36e178358809b5ad4ec04137ccb
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3162395
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3162395
Publikováno v:
Clinical Chemistry. 42:598-603
Multiple endocrine neoplasia type 2 (MEN 2) is an autosomal dominant cancer syndrome caused by mutations in the RET protooncogene. Others have already demonstrated the value of genetic testing in known MEN 2 kindreds. Previously described approaches
Autor:
Mark E. Nesbit, T. Kim, G D Hammond, H N Sather, L. L. Robison, Jorge A. Ortega, C A Sklar, A. T. Meadows
Publikováno v:
Journal of Clinical Oncology. 8:1981-1987
Testicular function was evaluated in 60 long-term survivors of childhood acute lymphoblastic leukemia (ALL). All the patients were treated on two consecutive Children Cancer Study Group protocols and received identical chemotherapy and either 18 or 2
Autor:
C A, Sklar, A C, Mertens, A, Walter, D, Mitchell, M E, Nesbit, M, O'Leary, R, Hutchinson, A T, Meadows, L L, Robison
Publikováno v:
Medical and pediatric oncology. 35(2)
The risk factors responsible for an increased prevalence of obesity or overweight in survivors of acute lymphoblastic leukemia (ALL) remain controversial. We evaluated changes in body mass index (BMI) in a cohort of ALL survivors, all of whom have be
Publikováno v:
Cancer. 78(9)
Multiple endocrine neoplasia type 2 (MEN 2) is a group of related autosomal dominant cancer syndromes caused by mutations in the RET protooncogene. A subset of familial Hirschsprung's disease, aganglionic megacolon, is also caused by mutations in thi
Autor:
C A, Sklar
Publikováno v:
Pediatrician. 18(1)
Linear growth and final adult stature in survivors of childhood cancer may be affected adversely by the disease itself as well as by the treatments utilized. The endocrine causes of impaired growth, which include growth hormone deficiency, primary th
Autor:
E. G. Garmey, Q. Liu, C. A. Sklar, L. R. Meacham, M. Stovall, Y. Yasui, L. L. Robison, K. C. Oeffinger
Publikováno v:
Journal of Clinical Oncology. 25:9518-9518
9518 Background: We previously reported an association between ≥ 20 Gy cranial radiotherapy (CRT) and obesity in adult survivors of childhood ALL. This follow-up study aimed to determine if, with time, (1) the prevalence of obesity and (2) the rate
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 52:9-16
We describe the results of clinical and endocrinological investigations performed on 10 children and adolescents (5 males and 5 females) with a primary central nervous system germinoma. Eight of 10 patients were between 10-20 yr of age at the time of
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 53:656-660
We report a 5 6/12-yr-old male who developed incomplete sexual precocity due to a hCG-secreting tumor in the region of the pineal gland. The patient presented with evidence of increased intracranial pressure (Parinaud's sign and papilledema) and was
Publikováno v:
Clinical Endocrinology. 14:311-320