Erika Leenders - Radboud Institute of Molecular Life Sciences (RIMLS), Radboud University Medical Center

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论文共 26 篇作者统计合作学者相似作者

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Trametinib Restores the Central Conducting Lymphatic Flow in a Premature Infant with Noonan Syndrome

Erika K S M Leenders,Lotte E R Kleimeier, Lauren C Weeke, Catelijne H Coppens,Willemijn M Klein,Jos M T Draaisma

Clinical case reportsno. 7 (2024): e9164-e9164

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Nerve Enlargement in Patients with Noonan Syndrome: A Retrospective Cohort Study

Fieke Draaisma,Erika K. S. M. Leenders,Corrie E. Erasmus,Hilde M. H. Braakman,Melanie C. J. Burgers, Catelijne H. Coppens,Tuula Rinne,Martin Zenker,Marco Tartaglia, Wesley Reintjes,Nicol C. Voermans,Baziel G. M. van Engelen,Nens van Alfen,Jos M. T. Draaisma

AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2024）

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Differentiating Primary Sarcomeric Hypertrophic Cardiomyopathy from Noonan Syndrome: Can the Electrocardiogram Be of Use

Robert W. L. Hauptmeijer, Lea Lippert,Floris E. A. Udink ten Cate,Zina Fejzic,Erika Leenders,Cordula M. Wolf,Jos M. T. Draaisma

CARDIOLOGY IN THE YOUNG（2024）

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Hypertrophic Neuropathy: a Possible Cause of Pain in Children with Noonan Syndrome and Related Disorders

Fieke Draaisma,Corrie E. Erasmus,Hilde M. H. Braakman,Melanie C. J. Burgers,Erika K. S. M. Leenders,Tuula Rinne,Nens van Alfen,Jos M. T. Draaisma

European journal of pediatricsno. 8 (2023): 3789-3793

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The most important problems and needs of rasopathy patients with a noonan syndrome spectrum disorder

Dagmar K Tiemens,Lotte Kleimeier,Erika Leenders,Ellen Wingbermühle,Renee L Roelofs,Barbara Sibbles,Floor S M Oostwegel,Eva Vroonland, Conny van Leeuwen, Hanneke Niessen, Paul Sonnega, Anniek Duursma,Michel A A P Willemsen,Jos M T Draaisma,Carina A C M Pittens

Orphanet journal of rare diseasesno. 1 (2023): 198-13

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Further delineation of the phenotype of Noonan syndrome with loose anagen hair due to de novo missense variants in the PPP1CB gene

Erika Leenders, Luisa Kocherscheid,Francesca Pantaleoni,Nathalie Pouvreau,Christina Lissewski,Susanne Kamphausen,Julia Brinkmann, Alice Bonnard,Denny Schanze,Marialisa Dentici,Maria Cristina Digilio,Laura Mazzanti,Hulya Kayserili,Pelin Ozlem Simsek-Kiper,Heide Seidel,Kerstin Kutsche, Nicole Fleisher,David Koolen,Brian Hon Yin Chung, Jasmine Fung,Austin Larson, Lysa Minasi,Tzung-Chien Hsieh,Peter Krawitz,Marwan Shinawi,Yolande Van Bever,Odile Boute,Hartmut Engels, Maike Grootenhaar,Tuula Rinne,Karen Gripp,Helene Cave,Marja Wessels,Alain Verloes,Marco Tartaglia,Martin Zenker

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 233-234

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TAB2 deletions and loss-of-function variants cause a Noonan-like syndrome with mitral valve disease, cardiomyopathy and hypermobility

Aafke Engwerda,Erika K. S. M. Leenders,Barbara Frentz,Paulien A. Terhal,Katharina Lohner,Bert B. A. De Vries, Trijnie Djikhuizen,Yvonne J. Vos,Tuula Rinne,Maarten P. Van den Berg,Marc T. R. Roofthooft,Patrick Deelen,Conny M. A. Van Ravenswaaij-Arts,Wilhelmina S. Kerstjens-Frederikse

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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Cognitive Phenotype and Psychopathology in Noonan Syndrome Spectrum Disorders through Various Ras/MAPK Pathway Associated Gene Variants

Ellen Wingbermuhle,Renee L. Roelofs,Wouter Oomens, Jennifer Kramer,Jos M. T. Draaisma,Erika Leenders,Tjitske Kleefstra,Roy P. C. Kessels,Jos I. M. Egger

JOURNAL OF CLINICAL MEDICINE（2022）

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