Zobrazeno 1 - 10
of 13
pro vyhledávání: '"A H, Shlossberg"'
Autor:
M L Givner, L Lehmann, R Douglas, E C Abbott, M H Tan, S R Salisbury, S E York, A H Shlossberg, S Reddy, R S Rittmaster
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 83:814-818
Medical treatment of Graves' disease involves antithyroid drugs with or without the addition of exogenous T4. There have been conflicting reports as to whether the addition of T4 improves remission rates or delays relapse. To evaluate this issue in a
Publikováno v:
European Journal of Endocrinology. 135:440-443
Loh K-C, Gupta R, Shlossberg AH. Spontaneous remission of ectopic Cushing's syndrome due to pheochromocytoma: a case report. Eur J Endocrinol 1996;135:440–3. ISSN 0804–4643 A young female adult with Cushing's syndrome arising from ectopic product
Autor:
S Reddy, M. H. Tan, R Douglas, Roger S. Rittmaster, S E York, Morris L. Givner, L Lehmann, Sonia R. Salisbury, H Zwicker, E. C. Abbott, M K Gupta, A. H. Shlossberg
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 81:3283-3288
Medical treatment of Graves' disease involves use of antithyroid drugs with or without the addition of exogenous L-T4. There have been conflicting reports as to whether the addition of T4 reduces TSH receptor antibodies and improves remission rates m
Publikováno v:
The Endocrinologist. 6:257-263
Autor:
A H, Shlossberg
Publikováno v:
Canadian family physician Medecin de famille canadien. 36
Recent advances in thyroid testing have simplified the approach to the screening and diagnosis of thyroid disorders. The metabolic state is best determined by the serum free thyroxine and a sensitive assay for serum thyroid-stimulating hormone. The p
Autor:
Bettina Lorenz-Depiereux, Mustapha Amyere, Ursula Müller-Barth, Miikka Vikkula, Stephanie M Kaiser, Janine Wagenstaller, José L. Olivares, Roger S. Rittmaster, Alan H Shlossberg, Klaus Badenhoop, Tim M. Strom, Harald Jüppner, César Loris, Feliciano J. Ramos, Anna Benet-Pagès, Murat Bastepe, Francis H. Glorieux
Publikováno v:
Nature Genetics, Vol. 38, no. 11, p. 1248-1250 (2006)
Hypophosphatemia is a genetically heterogeneous disease. Here, we mapped an autosomal recessive form (designated ARHP) to chromosome 4q21 and identified homozygous mutations in DMP1 (dentin matrix protein 1), which encodes a non-collagenous bone matr
Publikováno v:
QJM : monthly journal of the Association of Physicians. 90(1)
We retrospectively evaluated our experience with phaeochromocytoma from January 1986 to December 1995. There were 18 patients with surgically-proven phaeochromocytoma: three males, 15 females, aged 12-81 years (mean 42 years) at diagnosis. Sixteen we
Autor:
K C, Loh, A H, Shlossberg
Publikováno v:
Annals of the Academy of Medicine, Singapore. 25(6)
We report a case of a large macroprolactinoma in a 44-year-old male photographer who presented with affected colour perception and a central scotoma of the right eye. An initial computerised tomographic (CT) scan showed an enormous mass lesion extend
Autor:
A H, Shlossberg
Publikováno v:
Canadian family physician Medecin de famille canadien. 39
This article describes suggested treatment regimens for non-insulin-dependent diabetes mellitus. Diet is usually the first-line therapy. If this fails, most patients should be given a trial of oral agents, usually sulfonylurea first. Sulfonylurea and