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1.
Genotype in the diagnosis of 21-hydroxylase deficiency: who should undergo CYP21A2 analysis?
J Endocrinol Invest
; 36(11): 1083-9, 2013 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-24081139
2.
Diagnosis, genetic characterization and clinical follow up of mitochondrial fatty acid oxidation disorders in the new era of expanded newborn screening: A single centre experience.
Mol Genet Metab Rep
; 24: 100632, 2020 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-32793418
3.
A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis.
J Endocrinol Invest
; 31(1): 1-7, 2008 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-18296898
4.
Lack of association between thyrotropin receptor gene polymorphisms and subclinical hypothyroidism in children.
J Endocrinol Invest
; 30(2): 163-6, 2007 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-17392608
5.
Vitamin B12 Administration by Subcutaneous Catheter Device in a Cobalamin A (cblA) Patient.
JIMD Rep
; 35: 29-31, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-27858373
6.
[Influence of thyroid morphology on psychomotor development in patients with congenital hypothyroidism during 8 year follow-up]. / Influenza della morfologia tiroidea sullo sviluppo psicomotorio di bambini affetti da ipotiroidismo congenito durante 8 anni di follow-up.
Minerva Pediatr
; 62(3): 253-60, 2010 Jun.
Artículo
en Italiano
| MEDLINE | ID: mdl-20467377
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