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Konstantina Kosta

Showing results (1-10 of 8) with videos related to

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Hormones (Athens, Greece)|September 5, 2006
A boy with McCune-Albright syndrome associated with GH secreting pituitary microadenoma. Clinical findings and response to treatmentMaria Papadopoulou, Sofia Doula, Kostas Kitsios, et al.
Journal of Clinical Research in Pediatric Endocrinology|February 1, 2013
High-sensitivity C-reactive protein levels and metabolic disorders in obese and overweight children and adolescentsKonstantinos Kitsios, Maria Papadopoulou, Konstantina Kosta, et al.
American Journal of Human Genetics|September 12, 2007
A Bayesian approach to copy-number-polymorphism analysis in nuclear pedigreesKonstantina Kosta, Ian Sabroe, Jonathan Goke, et al.
Journal of Pediatric Hematology/Oncology|June 14, 2022
Bilateral Gonadoblastoma in a 6-Year-old Girl With Frasier Syndrome: Need for Early Preventive GonadectomyKonstantinos Kollios, Aristea Karipiadou, Maria Papagianni, et al.
Children (Basel, Switzerland)|June 2, 2021
The Synergistic Effects of a Complementary Physiotherapeutic Scheme in the Psychological and Nutritional Treatment in a Teenage Girl with Type 1 Diabetes Mellitus, Anxiety Disorder and Anorexia NervosaPelagia Tsakona, Vaios Dafoulis, Anastasios Vamvakis, et al.
Diabetes Technology & Therapeutics|July 24, 2019
The Beneficial Effect of the Mobile Application <i>Euglyca</i> in Children and Adolescents with Type 1 Diabetes Mellitus: A Randomized Controlled TrialChristos Chatzakis, Dimitrios Floros, Maria Papagianni, et al.
World Journal of Clinical Pediatrics|June 10, 2025
Clinical and genetic diagnosis and management of Silver-Russell syndrome: Report of four casesIlektra Toulia, Parthena Savvidou, Athina Ververi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 12, 2020
Late diagnosis of 3β-Hydroxysteroid dehydrogenase deficiency: the pivotal role of gas chromatography-mass spectrometry urinary steroid metabolome analysis and a novel homozygous nonsense mutation in the <i>HSD3B2</i> genePavlos Fanis, Vassos Neocleous, Konstantina Kosta, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Hormones (Athens, Greece)|September 5, 2006
A boy with McCune-Albright syndrome associated with GH secreting pituitary microadenoma. Clinical findings and response to treatmentMaria Papadopoulou, Sofia Doula, Kostas Kitsios, et al.
Journal of Clinical Research in Pediatric Endocrinology|February 1, 2013
High-sensitivity C-reactive protein levels and metabolic disorders in obese and overweight children and adolescentsKonstantinos Kitsios, Maria Papadopoulou, Konstantina Kosta, et al.
American Journal of Human Genetics|September 12, 2007
A Bayesian approach to copy-number-polymorphism analysis in nuclear pedigreesKonstantina Kosta, Ian Sabroe, Jonathan Goke, et al.
Journal of Pediatric Hematology/Oncology|June 14, 2022
Bilateral Gonadoblastoma in a 6-Year-old Girl With Frasier Syndrome: Need for Early Preventive GonadectomyKonstantinos Kollios, Aristea Karipiadou, Maria Papagianni, et al.
Children (Basel, Switzerland)|June 2, 2021
The Synergistic Effects of a Complementary Physiotherapeutic Scheme in the Psychological and Nutritional Treatment in a Teenage Girl with Type 1 Diabetes Mellitus, Anxiety Disorder and Anorexia NervosaPelagia Tsakona, Vaios Dafoulis, Anastasios Vamvakis, et al.
Diabetes Technology & Therapeutics|July 24, 2019
The Beneficial Effect of the Mobile Application <i>Euglyca</i> in Children and Adolescents with Type 1 Diabetes Mellitus: A Randomized Controlled TrialChristos Chatzakis, Dimitrios Floros, Maria Papagianni, et al.
World Journal of Clinical Pediatrics|June 10, 2025
Clinical and genetic diagnosis and management of Silver-Russell syndrome: Report of four casesIlektra Toulia, Parthena Savvidou, Athina Ververi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 12, 2020
Late diagnosis of 3β-Hydroxysteroid dehydrogenase deficiency: the pivotal role of gas chromatography-mass spectrometry urinary steroid metabolome analysis and a novel homozygous nonsense mutation in the <i>HSD3B2</i> genePavlos Fanis, Vassos Neocleous, Konstantina Kosta, et al.
Pageof 1