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Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis

Stayroula Papailiou

Stayroula Papailiou

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece
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Papailiou, Stayroula
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Elpis Athina Vlachopapadopoulou

Elpis Athina Vlachopapadopoulou

Department of Endocrinology, Growth and Development, ‘P. & A. Kyriakou Children’s HospitalAthens, Greece
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Vlachopapadopoulou, Elpis Athina
, 
Amalia Sertedaki

Amalia Sertedaki

Division of Endocrinology, Metabolism and Diabetes, First Department of Pediatrics, National and Kapodistrian University of Athens Medical School, ‘Aghia Sophia’ Children’s HospitalAthens, Greece
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Sertedaki, Amalia
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Despoina Maritsi

Despoina Maritsi

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece
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Maritsi, Despoina
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Nikolaos Syggelos

Nikolaos Syggelos

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece
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Syggelos, Nikolaos
 e 
Angeliki Syggelou

Angeliki Syggelou

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece
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Syggelou, Angeliki
  
27 ago 2020
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Pubblicato online: 27 ago 2020
Pagine: 227 - 229
DOI: https://doi.org/10.2478/enr-2020-0025
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© 2020 Stayroula Papailiou et al., published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Lingua:
Inglese
Frequenza di pubblicazione:
1 volte all'anno
Argomenti della rivista:
Scienze biologiche, Biologia molecolare, Neurobiologia, Medicina, Scienze medicali di base, Scienze medicali di base, altro, Medicina clinica, Medicina interna, Endocrinologia, Diabetologia
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