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1.
Joint associations between weekday and weekend physical activity or sedentary time and childhood obesity.
Int J Obes (Lond)
; 43(4): 691-700, 2019 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-30705394
2.
Low C0 and normal C16 and C18:1 masking the diagnosis of carnitine palmitoyltransferase II deficiency including a novel CPT2 variant: A case report.
Arch Pediatr
; 31(1): 85-88, 2024 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-38168614
3.
Two unrelated Chinese patients with hyperinsulinism /hyperammonemia (HI/HA) syndrome due to mutations in glutamate dehydrogenase gene.
J Pediatr Endocrinol Metab
; 23(7): 733-8, 2010 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-20857847
4.
Genetic characteristics and follow-up of patients with fatty acid ß-oxidation disorders through expanded newborn screening in a Northern Chinese population.
J Pediatr Endocrinol Metab
; 33(6): 683-690, 2020 May 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-32447334
5.
Identification and functional analysis of GCK gene mutations in 12 Chinese families with hyperglycemia.
J Diabetes Investig
; 10(4): 963-971, 2019 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-30592380
6.
The association between common genetic variation in the FTO gene and metabolic syndrome in Han Chinese.
Chin Med J (Engl)
; 123(14): 1852-8, 2010 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-20819567
7.
Protein causes hyperinsulinemia: a Chinese patient with hyperinsulinism/hyperammonaemia syndrome due to a glutamate dehydrogenase gene mutation.
Chin Med J (Engl)
; 123(13): 1793-5, 2010 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-20819649
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