Atrial septal defect often become more severe when encountered in genetic syndromes. Congenital disorder of glycosylation type 1a is an inherited metabolic disorder associated with mutations in PMM2 gene and can ...
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Σφακιανάκης Αλέξανδρος
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5 Άγιος Νικόλαος
Κρήτη 72100
00302841026182
00306932607174
alsfakia@gmail.com
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Τετάρτη 24 Ιανουαρίου 2018
Atrial septal defect in a patient with congenital disorder of glycosylation type 1a: a case report
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- Normative distribution of substance P and its tach...
- Retinal Arterio-Arterial Collaterals in Susac Synd...
- Literature Commentary
- Risk of Acute Ischemic Stroke in Patients With Mon...
- Serum irisin concentrations in lean adolescents wi...
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