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1.
Evidence of intrauterine growth restriction and growth hormone deficiency in 49,XXXXY syndrome.
Am J Med Genet A;
185(12): 3547-3553, 2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-32618131
2.
Concurrent diagnoses of Prader-Willi syndrome and GM2 gangliosidosis caused by uniparental disomy of chromosome 15.
Am J Med Genet A;
167A(8): 1944-8, 2015 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-25900722
3.
Update On The Clinical Perspectives And Care Of The Child With 47,XXY (Klinefelter Syndrome).
Appl Clin Genet;
12: 191-202, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31695472
4.
Short Stature in Chronic Kidney Disease Treated with Growth Hormone and an Aromatase Inhibitor.
Case Rep Pediatr;
2015: 738571, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26101681
5.
A 4-Year, Open-Label, Multicenter, Randomized Trial of Genotropin® Growth Hormone in Patients with Idiopathic Short Stature: Analysis of 4-Year Data Comparing Efficacy, Efficiency, and Safety between an Individualized, Target-Driven Regimen and Standard Dosing.
Horm Res Paediatr;
84(2): 79-87, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-25966824
6.
Kv1.3 channels are a therapeutic target for T cell-mediated autoimmune diseases.
Proc Natl Acad Sci U S A;
103(46): 17414-9, 2006 Nov 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-17088564
7.
Growth hormone deficiency in HIV-infected children following successful treatment with highly active antiretroviral therapy.
J Pediatr;
145(4): 549-51, 2004 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-15480383
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