Camelia Alkhzouz

Bone mineral density and bone turnover in Romanian children and young adults with classical 21‐hydroxylase deficiency are influenced by glucocorticoid replacement therapy

Anca Zimmermann, Paula Grigorescu Sido, Egbert Schulze et al. · Clinical Endocrinology · 2008 · 42 citations · Full text

Alterations in Lipid and Carbohydrate Metabolism in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Anca Zimmermann, Paula Grigorescu‐Sido, Camelia Alkhzouz et al. · Hormone Research in Paediatrics · 2010 · 36 citations

Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania

Călin Lazăr, Radu A. Popp, Adrian P. Trifa et al. · International Journal of Pediatric Otorhinolaryngology · 2010 · 23 citations

Mendelian Disorder, Genetic Disorder, Genetics +10

Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disability

Diana Miclea, Sergiu Oșan, Simona Bucerzan et al. · ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics · 2022 · 20 citations · Full text

Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study)

Simona Bucerzan, Diana Miclea, Radu A. Popp et al. · Therapeutics and Clinical Risk Management · 2017 · 19 citations · Full text