Found: 19
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Ultrasonographic evaluation of the median nerve at the level of the carpal tunnel outlet and mid forearm in patients with type II Mucopolysaccharidosis.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Association between Cardiac Malformations and Karyotype in Turner Syndrome - a Single Centre Study.
- Published in:
- Romanian Journal of Cardiology, 2021, v. 31, n. 4, p. 847, doi. 10.47803/rjc.2020.31.4.847
- By:
- Publication type:
- Article
The c.301_302delAG PROP1 gene mutation in Romanian patients with multiple pituitary hormone deficiency.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 9/10, p. 993, doi. 10.1515/jpem-2014-0289
- By:
- Publication type:
- Article
Hematological changes in patients with trisomy 21.
- Published in:
- Romanian Journal of Pediatrics / Revista Romana de Pediatrie, 2013, v. 62, n. 2, p. 185
- By:
- Publication type:
- Article
MODIFICĂRI HEMATOLOGICE LA PACIENȚII CU TRISOMIE 21.
- Published in:
- Romanian Journal of Pediatrics / Revista Romana de Pediatrie, 2013, v. 62, n. 2, p. 180
- By:
- Publication type:
- Article
Malformative syndrome in patients with trisomy 21.
- Published in:
- Romanian Journal of Pediatrics / Revista Romana de Pediatrie, 2012, v. 61, n. 4, p. 383
- By:
- Publication type:
- Article
SINDROMUL MALFORMATIV LA PACIENŢII CU TRISOMIE 21.
- Published in:
- Romanian Journal of Pediatrics / Revista Romana de Pediatrie, 2012, v. 61, n. 4, p. 379
- By:
- Publication type:
- Article
One Molecule for Mental Nourishment and More: Glucose Transporter Type 1—Biology and Deficiency Syndrome.
- Published in:
- Biomedicines, 2022, v. 10, n. 6, p. 1249, doi. 10.3390/biomedicines10061249
- By:
- Publication type:
- Article
Cardiac Manifestations in a Group of Romanian Patients with Gaucher Disease Type 1 (a Monocentric Study).
- Published in:
- Diagnostics (2075-4418), 2021, v. 11, n. 6, p. 989, doi. 10.3390/diagnostics11060989
- By:
- Publication type:
- Article
Cholelithiasis in Patients with Gaucher Disease type 1: Risk Factors and the Role of ABCG5/ABCG8 Gene Variants.
- Published in:
- Journal of Gastrointestinal & Liver Diseases, 2016, v. 25, n. 4, p. 447, doi. 10.15403/jgld.2014.1121.254.zim
- By:
- Publication type:
- Article
Bone mineral density and bone turnover in Romanian children and young adults with classical 21-hydroxylase deficiency are influenced by glucocorticoid replacement therapy.
- Published in:
- Clinical Endocrinology, 2009, v. 71, n. 4, p. 477, doi. 10.1111/j.1365-2265.2008.03518.x
- By:
- Publication type:
- Article
OSTEOARTHROPATHY IN MUCOPOLYSACCHARIDOSIS TYPE II.
- Published in:
- Clujul Medical, 2013, v. 86, n. 3, p. 270
- By:
- Publication type:
- Article
STRUCTURA ETIOPATOGENETICĂ A ARTROPATIILOR CRONICE LA COPIL.
- Published in:
- Clujul Medical, 2012, v. 85, n. 4, p. 634
- By:
- Publication type:
- Article
DISLIPIDEMIA LA COPIII ŞI ADOLESCENŢII OBEZI.
- Published in:
- Clujul Medical, 2010, v. 83, n. 1, p. 166
- By:
- Publication type:
- Article
POLIMORFISMUL APOPROTEINEI E LA PACIENŢII CU BOALĂGAUCHER TIP I.
- Published in:
- Clujul Medical, 2009, v. 82, n. 4, p. 586
- By:
- Publication type:
- Article
TULBURĂRI DE GLICOREGLARE LA COPIII ŞI ADOLESCENŢII OBEZI.
- Published in:
- Clujul Medical, 2009, v. 82, n. 4, p. 557
- By:
- Publication type:
- Article
ACIDOZA TUBULARĂ RENALĂ DISTALĂ - OBSERVAŢIA A DOUĂ CAZURI ÎNTR-O FRATRIE.
- Published in:
- Clujul Medical, 2009, v. 82, n. 3, p. 437
- By:
- Publication type:
- Article
Diagnosis and Management of Genetic Causes of Middle Aortic Syndrome in Children: A Comprehensive Literature Review.
- Published in:
- Therapeutics & Clinical Risk Management, 2022, v. 18, p. 233, doi. 10.2147/TCRM.S348366
- By:
- Publication type:
- Article
Rare complications of neurofibromatosis 1 diagnosed incidentally in two children.
- Published in:
- Therapeutics & Clinical Risk Management, 2018, v. 14, p. 1547, doi. 10.2147/TCRM.S173237
- By:
- Publication type:
- Article