Comparative meta‐analysis of Kabuki syndrome with and without hyperinsulinaemic hypoglycaemia-Reference-Cited by-同舟云学术

Comparative meta‐analysis of Kabuki syndrome with and without hyperinsulinaemic hypoglycaemia

Published:2020-07-15 Issue:3 Volume:93 Page:346-354
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Hoermann Henrike¹^ORCID,El‐Rifai Omar²³,Schebek Martin⁴,Lodefalk Maria⁵,Brusgaard Klaus³⁶,Bachmann Nadine⁷,Bergmann Carsten⁷,Roeper Marcia¹,Welters Alena¹,Salimi Dafsari Roschan¹,Blankenstein Oliver⁸,Mayatepek Ertan¹,Christesen Henrik²³⁹,Meissner Thomas¹,Kummer Sebastian¹

Affiliation:

1. Department of General Pediatrics, Neonatology and Pediatric Cardiology University Children’s Hospital DüsseldorfMedical Faculty Düsseldorf Germany

2. Hans Christian Andersen Children's Hospital Odense University Hospital Odense Denmark

3. Institute of Clinical Research University of Southern Denmark Odense Denmark

4. Department of Pediatric Diabetes Children's Hospital Kassel Kassel Germany

5. Department of Pediatrics Faculty of Medicine and Health Örebro University Örebro Sweden

6. Department of Clinical Genetics Odense University Hospital Odense Denmark

7. Center for Human Genetics Bioscientia Ingelheim Germany

8. Centre for Chronic Sick Children and Institute for Experimental Pediatric Endocrinology Charité‐Universitätsmedizin Berlin Berlin Germany

9. Odense Pancreas Centre OPAC Odense University Hospital Odense Denmark

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cen.14267

Reference34 articles.

1. Effects of Hypoglycemia on Developmental Outcome in Children With Congenital Hyperinsulinism

2. The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism

3. Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann, Sotos, and Kabuki syndromes: A nationwide survey in Japan

4. Congenital hyperinsulinism as the presenting feature of Kabuki syndrome: clinical and molecular characterization of 10 affected individuals

5. Beckwith–Wiedemann syndrome

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