Maria Maniati-Christidi

National and Kapodistrian University of Athens — Greece

Medicine · Health Sciences

12h-index567citations17works0.02yr avg
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Research Topics

Growth Hormone and Insulin-like Growth Factors(8), Sexual Differentiation and Disorders(8), Thyroid Disorders and Treatments(4), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities(4), Hormonal and reproductive studies(3)

Publications17 total

The spectrum of clinical, hormonal and molecular findings in 280 individuals with nonclassical congenital adrenal hyperplasia caused by mutations of the <i><scp>CYP</scp>21A2</i> gene
Clinical Endocrinology·2014· 84 cited
Spontaneous pregnancy and birth of a normal female from a woman with Turner syndrome and elevated gonadotropins
Fertility and Sterility·2005· 30 citedOpen Access
Growth Hormone Deficiency in a Child with Williams-Beuren Syndrome. The Response to Growth Hormone Therapy
Journal of Pediatric Endocrinology and Metabolism·2005· 9 cited
Ovulation induction and successful pregnancy outcome in two patients with Prop1 gene mutations
Fertility and Sterility·2004· 21 cited
Gene symbol: TSH B. Disease: congenital hypothyroidism.
PubMed·2004· 3 cited
Pituitary Magnetic Resonance Imaging in 15 Patients with Prop1 Gene Mutations: Pituitary Enlargement May Originate from the Intermediate Lobe
The Journal of Clinical Endocrinology & Metabolism·2004· 88 cited
Prolonged jaundice and hypothyroidism as the presenting symptoms in a neonate with a novel Prop1 gene mutation (Q83X)
European Journal of Endocrinology·2004· 28 citedOpen Access
Transient Congenital Hypothyroidism due to maternal autoimmune thyroid disease
HORMONES·2003· 36 citedOpen Access
Human Growth Hormone and Gonadotropin Releasing Hormone Analog Combination Therapy Increases Predicted Height in Short Normal Girls
Clinical Pediatrics·2003· 5 cited
Low TSH Congenital Hypothyroidism: Identification of a Novel Mutation of the TSH ß-Subunit Gene in One Sporadic Case (C85R) and of Mutation Q49stop in Two Siblings with Congenital Hypothyroidism
Pediatric Research·2002· 23 citedOpen Access
Early growth, pubertal development, body mass index and final height of patients with congenital adrenal hyperplasia: factors influencing the outcome
Clinical Endocrinology·2002· 97 cited
Insufficient Adrenarche in Patients with Combined Pituitary Hormone Deficiency Caused by a PROP A Gene Defect
Journal of Pediatric Endocrinology and Metabolism·2001· 17 cited
The Spectrum of Molecular Defects of the CYP21 Gene in the Hellenic Population: Variable Concordance between Genotype and Phenotype in the Different Forms of Congenital Adrenal Hyperplasia<sup>1</sup>
The Journal of Clinical Endocrinology & Metabolism·2001· 61 cited
Growth Response, Pubertal Growth and Final Height in Greek Children with Growth Hormone (GH) Deficiency on Long-term GH Therapy and Factors Affecting Outcome
Journal of Pediatric Endocrinology and Metabolism·2001· 15 cited
Genetic aspects of congenital adrenal hyperplasia.
PubMed·2001· 12 cited
The Growth Pattern and Final Height of Girls With Turner Syndrome With and Without Human Growth Hormone Treatment
PEDIATRICS·1998· 38 cited
152 THE RESPONSE OF PROLACTIN (PRL) AND GH TO L-DOPA IN OBESE CHILDREN AND ADOLESCENTS
Pediatric Research·1985Open Access

Frequent Co-authors

Catherine Dacou‐Voutetakis(17), Antonis Voutetakis(7), Amalia Sertedaki(7), Sarantis Livadas(7), Paraskevi Xekouki(3), Maria Dracopoulou(3), Maria I. Argyropoulou(2), Ioannis Bossis(2), Christina Kanaka‐Gantenbein(2), Maria Dracopoulou-Vabouli(2), Christina Kanaka‐Gantenbein(2), Irini Manoli(1), Ch. Kanaka-Gantenbein(1), Nicolas C. Thalassinos(1), Nicholas J. Patronas(1), Antonia Dastamani(1), Alexandra-Maria Magiakou(1), George P. Chrousos(1), Kiki Karavanaki-Karanassiou(1), Vasilis Petrou(1)