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1.
SLC2A1 Tag SNPs in Greek Patients with Diabetic Retinopathy and Nephropathy.
Ophthalmic Res
; 61(1): 26-35, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-29207384
2.
Hypertriglyceridemic Waist Phenotype and Its Association with Metabolic Syndrome Components, among Greek Children with Excess Body Weight.
Metabolites
; 13(2)2023 Feb 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-36837848
3.
A novel mutation in the AMHR2 gene, resulting in persistent Müllerian duct syndrome presenting with bilateral cryptorchidism and obstructed inguinal hernia.
J Pediatr Endocrinol Metab
; 36(9): 890-894, 2023 Sep 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-37480575
4.
Detection of hepatocyte nuclear factor 4A(HNF4A) gene variant as the cause for congenital hyperinsulinism leads to revision of the diagnosis of the mother.
J Pediatr Endocrinol Metab
; 34(4): 527-530, 2021 Apr 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-33031054
5.
Polycystic pancreatic disease associated with pineal cyst in an adolescent: a case report and literature overview.
Clin Case Rep
; 5(10): 1689-1691, 2017 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-29026573
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