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American Journal of Medical Genetics. Part A
|
January 6, 2023
Neonatal diagnosis of ACTA2-related disease: A case report and review of literature
Viviana Lupo, Maria Grazia Di Gregorio, Gerarda Mastrogiorgio, et al.
European Journal of Preventive Cardiology
|
May 23, 2018
Treatment of homozygous familial hypercholesterolaemia in paediatric patients: A monocentric experience
Paola S Buonuomo, Marina Macchiaiolo, Giovanna Leone, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
November 15, 2012
The celiac iceberg: characterization of the disease in primary schoolchildren
Raffaella Nenna, Claudio Tiberti, Laura Petrarca, et al.
Orphanet Journal of Rare Diseases
|
March 2, 2021
Clinical and molecular characterization of patients with adenylosuccinate lyase deficiency
Gerarda Mastrogiorgio, Marina Macchiaiolo, Paola Sabrina Buonuomo, et al.
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Search research articles
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Showing results (11-20 of 14) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 14 results.
American Journal of Medical Genetics. Part A
|
January 6, 2023
Neonatal diagnosis of ACTA2-related disease: A case report and review of literature
Viviana Lupo, Maria Grazia Di Gregorio, Gerarda Mastrogiorgio, et al.
European Journal of Preventive Cardiology
|
May 23, 2018
Treatment of homozygous familial hypercholesterolaemia in paediatric patients: A monocentric experience
Paola S Buonuomo, Marina Macchiaiolo, Giovanna Leone, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
November 15, 2012
The celiac iceberg: characterization of the disease in primary schoolchildren
Raffaella Nenna, Claudio Tiberti, Laura Petrarca, et al.
Orphanet Journal of Rare Diseases
|
March 2, 2021
Clinical and molecular characterization of patients with adenylosuccinate lyase deficiency
Gerarda Mastrogiorgio, Marina Macchiaiolo, Paola Sabrina Buonuomo, et al.
Page
of 2