Výsledky vyhledávání - Thomas Vulsma
- Zobrazuji výsledky 1 - 11 z 11
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Inactivating Mutations in the Gene for Thyroid Oxidase 2 (<i>THOX2</i>) and Congenital Hypothyroidism Autor J.C. Moreno, Hennie Bikker, Marlies Kempers, A.S. Paul van Trotsenburg, Frank Baas, Jan J. M. de Vijlder, Thomas Vulsma, Carrie Ris‐Stalpers
Vydáno 2002Artigo -
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Effects of Thyroxine Supplementation on Neurologic Development in Infants Born at Less Than 30 Weeks' Gestation Autor Aleid G. van Wassenaer, Joke H. Kok, Jan J. M. de Vijlder, Judy M. Briët, Bert J. Smit, Pieter Tamminga, Anneloes L. van Baar, Friedo W. Dekker, Thomas Vulsma
Vydáno 1997Artigo -
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The Effect of Thyroxine Treatment Started in the Neonatal Period on Development and Growth of Two-Year-Old Down Syndrome Children: A Randomized Clinical Trial Autor A.S. Paul van Trotsenburg, Thomas Vulsma, Susanne L. Rutgers van Rozenburg-Marres, Anneloes L. van Baar, Jeannette C. D. Ridder, H. S. A. Heymans, Jan G.P. Tijssen, Jan J. M. de Vijlder
Vydáno 2005Artigo -
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Neonatal Screening for Congenital Hypothyroidism in The Netherlands: Cognitive and Motor Outcome at 10 Years of Age Autor Marlies Kempers, Liesbeth van der Sluijs Veer, Maria W. G. Nijhuis‐van der Sanden, C.I. Lanting, Libbe Kooistra, Brenda M. Wiedijk, Bob F. Last, Jan J. M. de Vijlder, Martha A. Grootenhuis, Thomas Vulsma
Vydáno 2006Artigo -
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Normalization of Height in Girls with Turner Syndrome after Long-Term Growth Hormone Treatment: Results of a Randomized Dose-Response Trial<sup>1</sup> Autor Theo Sas, Sabine M.P.F. de Muinck Keizer‐Schrama, Theo Stijnen, M. Jansen, Barto J. Otten, J. J. Gera Hoorweg-Nijman, Thomas Vulsma, Guy Massa, Catrienus W. Rouwé, H.M. Reeser, Willem‐Jan M. Gerver, Jos J. Gosen, C. Rongen‐Westerlaken, Stenvert L. S. Drop
Vydáno 1999Artigo -
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Final Height in Girls with Turner Syndrome after Long-Term Growth Hormone Treatment in Three Dosages and Low Dose Estrogens Autor Yvonne K. van Pareren, Sabine M.P.F. de Muinck Keizer‐Schrama, Theo Stijnen, Theo Sas, M. Jansen, Barto J. Otten, J. J. Gera Hoorweg-Nijman, Thomas Vulsma, Wilhelmina H. Stokvis‐Brantsma, Catrienus W. Rouwé, H.M. Reeser, Willem‐Jan M. Gerver, Jos J. Gosen, C. Rongen‐Westerlaken, Stenvert L. S. Drop
Vydáno 2003Artigo -
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Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement Autor Yu Sun, Beata Bąk, Nadia Schoenmakers, A.S. Paul van Trotsenburg, Wilma Oostdijk, Peter J. Voshol, Emma L. Cambridge, Jacqueline K. White, Paul Le Tissier, S. Neda Mousavy Gharavy, Juan Pedro Martı́nez-Barberá, Wilhelmina H. Stokvis‐Brantsma, Thomas Vulsma, Marlies Kempers, Luca Persani, Irene Campi, Marco Bonomi, Paolo Beck‐Peccoz, Hongdong Zhu, Timothy M. E. Davis, Anita Hokken-Koelega, Darya Gorbenko del Blanco, Jayanti Rangasami, Claudia Ruivenkamp, Jeroen F. J. Laros, Marjolein Kriek, Sarina G. Kant, Cathy A.J. Bosch, Nienke R. Biermasz, Natasha M. Appelman‐Dijkstra, Eleonora P.M. Corssmit, Guido C. Hovens, Alberto M. Pereira, Johan T. den Dunnen, Michael G. Wade, Martijn H. Breuning, Raoul C. M. Hennekam, Krishna Chatterjee, Mehul Dattani, Jan M. Wit, Daniel J. Bernard
Vydáno 2012Artigo
Vyhledávací nástroje:
Související témata
Medicine
Internal medicine
Endocrinology
Biology
Hormone
Pediatrics
Thyroid
Congenital hypothyroidism
Genetics
Central hypothyroidism
Confidence interval
Gene
Randomized controlled trial
Biochemistry
Cognition
Cohort
Enzyme
Growth hormone
Pregnancy
Prospective cohort study
Psychiatry
Short stature
Thyrotropin-releasing hormone
Turner syndrome
16S ribosomal RNA
Adverse effect
Alternative medicine
Anterior pituitary
Antithyroid agent
Bayley Scales of Infant Development