One Molecule for Mental Nourishment and More: Glucose Transporter Type 1—Biology and Deficiency Syndrome von Vulturar, Romana, Chiș, Adina, Pintilie, Sebastian, Farcaș, Ilinca Maria, Botezatu, Alina, Login, Cristian Cezar, Sitar-Taut, Adela-Viviana, Orasan, Olga Hilda, Stan, Adina, Lazea, Cecilia, Al-Khzouz, Camelia, Mager, Monica, Vințan, Mihaela Adela, Manole, Simona, Damian, Laura

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Prevalence of ∆F508 cystic fibrosis carriers in a Romanian population group von Osan, Sergiu Nicolae, Hrapsa, Iona, Coroama, Constantin Ionut, Miclea, Diana Laura, Al-Khzouz, Camelia, Lazar, Calin, Farcas, Marius Florin

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Cardiac Manifestations in a Group of Romanian Patients with Gaucher Disease Type 1 (a Monocentric Study) von Lazea, Cecilia, Bucerzan, Simona, Al-Khzouz, Camelia, Zimmermann, Anca, Vesa, Ștefan Cristian, Nașcu, Ioana, Creț, Victoria, Crișan, Mirela, Asăvoaie, Carmen, Miclea, Diana, Grigorescu-Sido, Paula

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GJB2 and GJB6 genes mutations in children with non-syndromic hearing loss von Lazăr, Călin, Popp, Radu, Al-Khzouz, Camelia, Mihuț, Gheorghe, Grigorescu-Sido, Paula

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Diagnosis and Management of Genetic Causes of Middle Aortic Syndrome in Children: A Comprehensive Literature Review von Lazea, Cecilia, Al-Khzouz, Camelia, Sufana, Crina, Miclea, Diana, Asavoaie, Carmen, Filimon, Ioana, Fufezan, Otilia

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Rare complications of neurofibromatosis 1 diagnosed incidentally in two children von Lazea, Cecilia, Asavoaie, Carmen, Al-Khzouz, Camelia, Popa, Lenuta

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Bone mineral density and bone turnover in Romanian children and young adults with classical 21-hydroxylase deficiency are influenced by glucocorticoid replacement therapy von Zimmermann, Anca, Sido, Paula Grigorescu, Schulze, Egbert, Al Khzouz, Camelia, Lazea, Cecilia, Coldea, Cristina, Weber, Matthias M.

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Cholelithiasis in Patients with Gaucher Disease type 1: Risk Factors and the Role of ABCG5/ABCG8 Gene Variants von Zimmermann, Anca, Popp, Radu A, Al-Khzouz, Camelia, Bucerzan, Simona, Naşcu, Ioana, Leucuta, Daniel, Galle, Peter R., Grigorescu-Sido, Paula

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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 von Bocsa, Corina, Asavoaie, Carmen, Bucerzan, Simona, Nascu, Ioana, Brumboiu, Irina, Al-Khzouz, Camelia

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Dynamic changes of lipid profile in Romanian patients with Gaucher disease type 1 under enzyme replacement therapy: a prospective study von Zimmermann, Anca, Grigorescu-Sido, Paula, Rossmann, Heidi, Lackner, Karl J., Drugan, Cristina, Al Khzouz, Camelia, Bucerzan, Simona, Naşcu, Ioana, Zimmermann, Tim, Leucuţa, Daniel, Weber, Matthias M.

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Osteoarthropathy in mucopolysaccharidosis type II von Nascu, Ioana, Grigorescu-Sido, Paula, Al-Khzouz, Camelia, Bucerzan, Simona, Denes, Carmencita, Lazea, Cecilia

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Cardiovascular manifestations in Marfan syndrome von Lazea, Cecilia, Bucerzan, Simona, Crisan, Mirela, Al-Khzouz, Camelia, Miclea, Diana, Şufană, Crina, Cismaru, Gabriel, Grigorescu-Sido, Paula

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MODIFICĂRI HEMATOLOGICE LA PACIENŢII CU TRISOMIE 21 von Raluca Maria Vlad, Paula Grigorescu Sido, Simona Bucerzan, Camelia Al-Khzouz, Ioana Naşcu, Eugen Pascal Ciofu

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SINDROMUL MALFORMATIV LA PACIENŢII CU TRISOMIE 21 von Raluca Maria Vlad, Paula Grigorescu Sido, Simona Bucerzan, Camelia Al-Khzouz, Ioana Naşcu, Eugen Pascal Ciofu

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