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1.
A novel stop codon variant affecting ΔNp63 isoforms associated with non-syndromic limb-mammary phenotype and uterine cervix dysplasia.
Clin Genet
; 99(3): 486-487, 2021 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-33258108
2.
Turner Syndrome: Pitfalls of Transition from Paediatric to Adult Health Care.
Endocr Metab Immune Disord Drug Targets
; 2024 May 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-38808721
3.
Transition from pediatrics to adult health care in girls with turner syndrome.
Expert Rev Endocrinol Metab
; 19(3): 229-240, 2024 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-38664997
4.
Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.
Front Endocrinol (Lausanne)
; 15: 1382583, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38737552
5.
The Italian registry for patients with Prader-Willi syndrome.
Orphanet J Rare Dis
; 18(1): 28, 2023 02 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-36793093
6.
First Year Metabolic and Hormonal Behavior Define two Different Populations of SGA Newborn for Weight or Height.
J Endocr Soc
; 6(5): bvac028, 2022 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35350393
7.
Important Tools for Use by Pediatric Endocrinologists in the Assessment of Short Stature
J Clin Res Pediatr Endocrinol
; 13(2): 124-135, 2021 06 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33006554
8.
Summary of Expert Opinion on the Management of Children With Chronic Kidney Disease and Growth Failure With Human Growth Hormone.
Front Endocrinol (Lausanne)
; 11: 587, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33013690
9.
Growth Trajectory and Adult Height in Children with Nonclassical Congenital Adrenal Hyperplasia.
Horm Res Paediatr
; 93(3): 173-181, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32810858
10.
[Usefulness of the 5-6-yrs-old anthropometric health report for the evaluation of childhood overweight and obesity: pilot study in Lombardia (Italy)]. / Utilità della scheda bilancio di salute per la rilevazione di sovrappeso e obesità nei bambini tra 5 e 6 anni: esperienza pilota in Lombardia.
Epidemiol Prev
; 31(1): 56-61, 2007.
Artículo
en Italiano
| MEDLINE | ID: mdl-17591405
11.
A novel deletion in the GH1 gene including the IVS3 branch site responsible for autosomal dominant isolated growth hormone deficiency.
J Clin Endocrinol Metab
; 91(3): 980-6, 2006 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-16368751
12.
Stories of experiences of care for growth hormone deficiency: the CRESCERE project.
Future Sci OA
; 2(1): FSO82, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-28031934
13.
Long-term safety and efficacy of Omnitrope®, a somatropin biosimilar, in children requiring growth hormone treatment: Italian interim analysis of the PATRO Children study.
Ital J Pediatr
; 42(1): 93, 2016 Nov 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-27809913
14.
The insulin-like growth factor-II receptor gene is associated with type 1 diabetes: evidence of a maternal effect.
J Clin Endocrinol Metab
; 89(11): 5700-6, 2004 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-15531531
15.
Limb-mammary syndrome (LMS) associated with internal female genitalia dysgenesia: a new genotype/phenotype correlation?
Am J Med Genet A
; 146A(15): 2001-4, 2008 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-18627043
16.
Mechanisms and management of growth impairment in children affected by inflammatory bowel disease.
Expert Rev Endocrinol Metab
; 8(3): 289-299, 2013 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-30780818
17.
T lymphocyte maturation is impaired in healthy young individuals carrying trisomy 21 (Down syndrome).
Am J Intellect Dev Disabil
; 114(2): 100-9, 2009 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-19391670
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