检索结果 - Nitash Zwaveling‐Soonawala

  • Showing 1 - 11 results of 11
Refine Results
  1. 1
    The Severity of Congenital Hypothyroidism of Central Origin Should Not Be Underestimated

    The Severity of Congenital Hypothyroidism of Central Origin Should Not Be Underestimated 由 Nitash Zwaveling‐Soonawala, A.S. Paul van Trotsenburg, P.H. Verkerk

    出版 2014
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  2. 2
    Neonatal screening for primary and central congenital hypothyroidism: is it time to go Dutch?

    Neonatal screening for primary and central congenital hypothyroidism: is it time to go Dutch? 由 Anita Boelen, Nitash Zwaveling‐Soonawala, Annemieke C. Heijboer, A.S. Paul van Trotsenburg

    出版 2023
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  3. 3
    Methimazole-induced remission rates in pediatric Graves’ disease: a systematic review

    Methimazole-induced remission rates in pediatric Graves’ disease: a systematic review 由 Jelmer M van Lieshout, Christiaan F. Mooij, A.S. Paul van Trotsenburg, Nitash Zwaveling‐Soonawala

    出版 2021
    获取全文
    Revisão
    加到收藏夹
    Saved in:
  4. 4
    Diagnosis and Management of Central Congenital Hypothyroidism

    Diagnosis and Management of Central Congenital Hypothyroidism 由 Peter Lauffer, Nitash Zwaveling‐Soonawala, Jolanda C. Naafs, Anita Boelen, A.S. Paul van Trotsenburg

    出版 2021
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  5. 5
    Newborn screening for congenital hypothyroidism: worldwide coverage 50 years after its start

    Newborn screening for congenital hypothyroidism: worldwide coverage 50 years after its start 由 Marta Arrigoni, Nitash Zwaveling‐Soonawala, Stephen LaFranchi, A.S. Paul van Trotsenburg, Christiaan F. Mooij

    出版 2025
    获取全文
    Revisão
    加到收藏夹
    Saved in:
  6. 6
    Clues for Polygenic Inheritance of Pituitary Stalk Interruption Syndrome From Exome Sequencing in 20 Patients

    Clues for Polygenic Inheritance of Pituitary Stalk Interruption Syndrome From Exome Sequencing in 20 Patients 由 Nitash Zwaveling‐Soonawala, Mariëlle Alders, Aldo Jongejan, Lidija Kovačič, Floor A.M. Duijkers, Saskia M. Maas, Eric Fliers, A.S. Paul van Trotsenburg, Raoul C. M. Hennekam

    出版 2017
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  7. 7
    Mutations in <i>TBL1X</i> Are Associated With Central Hypothyroidism

    Mutations in <i>TBL1X</i> Are Associated With Central Hypothyroidism 由 Charlotte A. Heinen, Monique Losekoot, Yu Sun, Peter J. Watson, Louise Fairall, Sjoerd D. Joustra, Nitash Zwaveling‐Soonawala, Wilma Oostdijk, Erica L T van den Akker, Mariëlle Alders, Gijs W.E. Santen, Rick R. van Rijn, Wouter A. Dreschler, Olga V. Surovtseva, Nienke R. Biermasz, Raoul C. M. Hennekam, Jan M. Wit, John W. R. Schwabe, Anita Boelen, Eric Fliers, A.S. Paul van Trotsenburg

    出版 2016
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  8. 8
    Bone Mineral Density in Children and Adolescents With Prader-Willi Syndrome: A Longitudinal Study During Puberty and 9 Years of Growth Hormone Treatment

    Bone Mineral Density in Children and Adolescents With Prader-Willi Syndrome: A Longitudinal Study During Puberty and 9 Years of Growth Hormone Treatment 由 Nienke Bakker, Renske Kuppens, Elbrich P. C. Siemensma, Roderick F. A. Tummers-de Lind van Wijngaarden, Dederieke A. M. Festen, G. C. B. Bindels-de Heus, Gianni Bocca, Danny A. J. P. Haring, J. J. Gera Hoorweg-Nijman, E. C. A. M. Houdijk, Petr Jira, L. Lunshof, Roelof J. Odink, Wilma Oostdijk, Joost Rotteveel, A. A. E. M. Van Alfen, Mariëtte van Leeuwen, Hester van Wieringen, M. E. J. Wegdam-den Boer, Nitash Zwaveling‐Soonawala, Anita Hokken-Koelega

    出版 2015
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  9. 9
    Eight Years of Growth Hormone Treatment in Children With Prader-Willi Syndrome: Maintaining the Positive Effects

    Eight Years of Growth Hormone Treatment in Children With Prader-Willi Syndrome: Maintaining the Positive Effects 由 Nienke Bakker, Renske Kuppens, Elbrich P. C. Siemensma, Roderick F. A. Tummers-de Lind van Wijngaarden, Dederieke A. M. Festen, G. C. B. Bindels-de Heus, Gianni Bocca, Danny A. J. P. Haring, J. J. Gera Hoorweg-Nijman, E. C. A. M. Houdijk, Petr Jira, L. Lunshof, Roelof J. Odink, Wilma Oostdijk, Joost Rotteveel, Eelco J. Schroor, A. A. E. M. Van Alfen, Mariëtte van Leeuwen, Evelyn van Pinxteren-Nagler, Hester van Wieringen, René C. F. M. Vreuls, Nitash Zwaveling‐Soonawala, Maria de Ridder, Anita C. S. Hokken‐Koelega

    出版 2013
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  10. 10
    Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

    Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study 由 Stefan Groeneweg, van Geest FS, Ayhan Abacı, Alberto Alcantud, Ambegaonkar GP, Armour CM, Parkash A. Bakhtiani, Diana Bârcă, Bertini ES, van Beynum Im, Nicola Brunetti‐Pierri, Massimiliano Bugiani, Marco Cappa, Gerarda Cappuccio, Barbara Castellotti, Carlotta Castiglioni, Krishnarpan Chatterjee, de Coo IFM, Régis Coutant, Dana Craiu, Patricia Crock, Christian DeGoede, Koray Demir, Alice Dica, Paul Dimitri, Anna Dolcetta‐Capuzzo, Dremmen MHG, Rachana Dubey, Anina Enderli, Jan Fairchild, Jonathan Gallichan, Biju George, Gevers EF, Annette Hackenberg, Zita Halász, B. Heinrich, Thao Huynh, Anna Kłosowska, van der Knaap, van der Knoop, Daniel Konrad, Koolen DA, Heiko Krude, Amy Lawson‐Yuen, Jan Lebl, M Linder-Lucht, Lorea CF, Lourenco CM, RJ Lunsing, G Lyons, Jana Malíková, Mancilla EE, Aaron McGowan, Verónica Mericq, Lora FM, Cassandra Moran, Muller Ke, Isabelle Oliver‐Petit, Laura Paone, Paul PG, Michel Polak, Francesco Porta, Poswar FO, Christina Reinauer, Klára Roženková, Menevse TS, Peter Simm, András Simon, Yogesh Preet Singh, Marco Spada, van der Spek J, Stals MAM, Athanasia Stoupa, Subramanian GM, Davide Tonduti, Serkan Turan, den Uil CA, Joel A. Vanderniet, van der Walt A, Wémeau Jl, Jolanta Wierzba, de Wit MY, Nicole I. Wolf, Michael Wurm, Federica Zibordi, Amnon Zung, Nitash Zwaveling‐Soonawala, Visser WE

    出版 2021
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  11. 11
    Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

    Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study 由 Stefan Groeneweg, Ferdy S. van Geest, Ayhan Abacı, Alberto Alcantud, Gautam Ambegaonkar, Christine M. Armour, Priyanka Bakhtiani, Diana Bârcă, Enrico Bertini, Ingrid M. van Beynum, Nicola Brunetti‐Pierri, Marianna Bugiani, Marco Cappa, Gerarda Cappuccio, Barbara Castellotti, Claudia Castiglioni, Krishna Chatterjee, I.F.M. de Coo, Régis Coutant, Dana Craiu, Patricia Crock, Christian DeGoede, Korcan Demir, Alice Dica, Paul Dimitri, Anna Dolcetta‐Capuzzo, Marjolein H. G. Dremmen, Rachana Dubey, Anina Enderli, Jan Fairchild, Jonathan Gallichan, Belinda George, Evelien Gevers, Annette Hackenberg, Zita Halász, Bianka Heinrich, Tony Huynh, Anna Kłosowska, Marjo S. van der Knaap, Marieke M van der Knoop, Daniel Konrad, David A. Koolen, Heiko Krude, Amy Lawson‐Yuen, Jan Lebl, M Linder-Lucht, Cláudia Fernandes Lorea, Charles Marques Lourenço, Roelineke J. Lunsing, Greta Lyons, Jana Malíková, Edna E. Mancilla, Anne McGowan, Verónica Mericq, Felipe Monti Lora, Carla Moran, Katalin Eszter Müller, Isabelle Oliver‐Petit, Laura Paone, Praveen George Paul, Michel Polak, Francesco Porta, Fabiano O. Poswar, Christina Reinauer, Klára Roženková, tuba seven menevse, Peter Simm, Anna Simon, Yogen Singh, Marco Spada, Jet van der Spek, Milou A.M. Stals, Athanasia Stoupa, Gopinath M. Subramanian, Davide Tonduti, Serap Turan, Corstiaan A. den Uil, Joel A. Vanderniet, Adri van der Walt, Jean‐Louis Wémeau, Jolante Wierzba, Marie‐Claire Y. de Wit, Nicole I. Wolf, Michael Wurm, Federica Zibordi, Amnon Zung, Nitash Zwaveling‐Soonawala, W. Edward Visser

    出版 2020
    获取全文
    Artigo
    加到收藏夹
    Saved in:

检索工具: