Found: 9
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3-HMG Coenzyme A Lyase Deficiency: Macrocephaly and Left Ventricular Noncompaction with a Novel Mutation.
- Published in:
- Indian Journal of Pediatrics, 2015, v. 82, n. 7, p. 645, doi. 10.1007/s12098-015-1722-6
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- Article
Molecular and clinical findings of Turkish patients with hereditary fructose intolerance.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2021, v. 34, n. 8, p. 1017, doi. 10.1515/jpem-2021-0303
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- Publication type:
- Article
The Relationship between Vitamin D Receptor Gene Polymorphisms and Bone Density, Osteocalcin Level and Growth in Adolescents.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2010, v. 23, n. 5, p. 491
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- Article
Stepwise diet management in pediatric gastrointestinal graft versus host disease.
- Published in:
- Turkish Journal of Pediatrics, 2016, v. 58, n. 2, p. 145, doi. 10.24953/turkjped.2016.02.004
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- Article
Viral etiology in infants hospitalized for acute bronchiolitis.
- Published in:
- Turkish Journal of Pediatrics, 2015, v. 57, n. 5, p. 592
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- Publication type:
- Article
Viral etiology in infants hospitalized for acute bronchiolitis.
- Published in:
- Turkish Journal of Pediatrics, 2014, v. 56, n. 6, p. 592
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- Publication type:
- Article
Reversible pulmonary arterial hypertension in cobalamin-dependent cobalamin C disease due to a novel mutation in the MMACHC gene.
- Published in:
- European Journal of Pediatrics, 2014, v. 173, n. 12, p. 1707, doi. 10.1007/s00431-014-2330-6
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- Article
Hypertrophic Cardiomyopathy with Familial Chylomicronemia Syndrome: Is it an Incidental Finding or a New Association?
- Published in:
- 2014
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- Publication type:
- Letter
The Association Between Vitamin D Status and Recurrent Wheezing.
- Published in:
- Indian Journal of Pediatrics, 2013, v. 80, n. 11, p. 907, doi. 10.1007/s12098-013-1005-z
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- Publication type:
- Article