Behaviour at 2 years of age in very preterm infants (gestational age <32 weeks)

Autor: GMSJ Stoelhorst, SE Martens, M Rijken, van Zwieten PHT, AH Zwinderman, JM Wit, S Veen

Publikováno v: Acta Paediatrica. 92:1-1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dd374672b29a2f0b6ee9dfa764abfdc8
https://doi.org/10.1080/08035350310011551

Insulinomas in MEN-I patients: early detection and treatment of insulinomas in patients with the multiple endocrine neoplasia syndrome type-I

Autor: Jadoul M, Hp, Koppeschaar, Ma, Bax, Wp, Mali, Jm, Wit, Huber J, Hans Vasen, Van der Sluys Veer J, Struyvenberg A, Cj, Lips

Publikováno v: Europe PubMed Central

In the multiple endocrine neoplasia syndrome type I (MEN-I syndrome), periodic screening of patients and their close relatives may improve prognosis and life expectancy. Although there is diffuse involvement of the pancreas with microadenomatosis, in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::fbcf416baf97a961ee6b3cf5e20ea657
http://europepmc.org/abstract/med/1979152

METHIONYL GROWTH HORMONE (met-GH) IN A DOSAGE OF 4 IU/m2 DAY PROMOTES GROWTH IN TURNER SYNDROME

Autor: M. Gons, B.J. Otten, Ha Delemarre-van de Wall, Jm Wit, C Rongen-Westerlaken, Sls Drop, W. Oostdijk

Publikováno v: Pediatric Research. 23:126-126

METHIONYL GROWTH HORMONE (met-GH) IN A DOSAGE OF 4 IU/m 2 DAY PROMOTES GROWTH IN TURNER SYNDROME

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::327ffe0f2f22a8bc903890476210236e
https://doi.org/10.1203/00006450-198801000-00150

Genetic Findings in Short Turkish Children Born to Consanguineous Parents.

Autor: Joustra SD; Department of Paediatrics, Division of Pediatric Endocrinology, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, The Netherlands., Isik E; Department of Paediatrics, Ankara Bilkent City Hospital, Ankara, Turkey., Wit JM; Department of Paediatrics, Division of Pediatric Endocrinology, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, The Netherlands., Catli G; Department of Paediatric Endocrinology, Izmir Katip Celebi University Faculty of Medicine, Izmir, Turkey.; Department of Paediatric Endocrinology, Istinye University Faculty of Medicine, Istanbul, Turkey., Anik A; Department of Paediatric Endocrinology, Dokuz Eylul University, Izmir, Turkey., Haliloglu B; Department of Paediatric Endocrinology and Diabetology, Marmara University School of Medicine, Istanbul, Turkey., Kandemir N; Department of Paediatric Endocrinology, Hacettepe University, Faculty of Medicine, Ankara, Turkey., Ozsu E; Department of Paediatric Endocrinology and Diabetes, University of Ankara, Ankara, Turkey., Hendriks YMC; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands., de Bruin C; Department of Paediatrics, Division of Pediatric Endocrinology, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, The Netherlands., Kant SG; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands., Campos-Barros A; Institute of Medical and Molecular Genetics (INGEMM), IdiPAZ, Hospital Universitario La Paz, Madrid, Spain.; Rare Diseases Biomedical Research Network (CIBERER; U 753), ISCIII, Madrid, Spain., Challis RC; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK., Parry D; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK., Harley ME; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK., Jackson A; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK., Losekoot M; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands., van Duyvenvoorde HA; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.

Publikováno v: Hormone research in paediatrics [Horm Res Paediatr] 2024 Jun 05, pp. 1-11. Date of Electronic Publication: 2024 Jun 05.

Identification of novel genes including NAV2 associated with isolated tall stature.

Autor: Weiss B; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany., Ott T; Department of Zoology, University of Hohenheim, Stuttgart, Germany., Vick P; Department of Zoology, University of Hohenheim, Stuttgart, Germany., Lui JC; National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, United States., Roeth R; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany., Vogel S; Department of Zoology, University of Hohenheim, Stuttgart, Germany., Waldmüller S; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany., Hoffmann S; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany., Baron J; National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, United States., Wit JM; Division of Pediatric Endocrinology, Department of Pediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, Netherlands., Rappold GA; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.

Publikováno v: Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2023 Dec 12; Vol. 14, pp. 1258313. Date of Electronic Publication: 2023 Dec 12 (Print Publication: 2023).