Resultados de procura - Rutger Jan Nievelstein
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A study of the clinical and radiological features in a cohort of 93 patients with a <i>COL2A1</i> mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype por Paulien A. Terhal, Rutger Jan Nievelstein, Eva J. J. Verver, Vedat Topsakal, Paula van Dommelen, Kristien Hoornaert, Martine Le Merrer, Andreas Zankl, Marleen Simon, Sarah Smithson, Carlo Marcelis, Bronwyn Kerr, Jill Clayton‐Smith, Esther Kinning, Sahar Mansour, Frances Elmslie, Linda Goodwin, Annemarie H. van der Hout, Hermine E. Veenstra‐Knol, Johanna C. Herkert, Allan M. Lund, Raoul C. M. Hennekam, André Mégarbané, Melissa Lees, Louise C. Wilson, Alison Male, Jane A. Hurst, Yasemin Alanay, Göran Annerén, Regina C. Betz, Ernie M.H.F. Bongers, Valérie Cormier‐Daire, Anne Dieux, Albert David, Mariet W. Elting, Jenneke van den Ende, Andrew Green, Johanna M. van Hagen, Niels Thomas Hertel, Muriel Holder‐Espinasse, Nicolette S. den Hollander, Tessa Homfray, Hanne Hove, Susan Price, Annick Raas‐Rothschild, Marianne Rohrbach, Barbara Schroeter, Mohnish Suri, Elizabeth M. Thompson, Edward S. Tobias, Annick Toutain, Maaike Vreeburg, Emma Wakeling, Nine Knoers, Paul Coucke, Geert Mortier
Publicado 2015Artigo
Ferramentas de procura:
Materias Relacionadas
Biology
Genetics
Medicine
Anesthesia
Asphyxia
Clinical phenotype
Cohort
Dysplasia
Gene
Gestational age
Hematoma
Intraventricular hemorrhage
Mutation
Neonatal intensive care unit
Neuroimaging
Neurology
Neuroradiology
Neurosurgery
Osteochondrodysplasia
Pathology
Pediatrics
Perinatal asphyxia
Phenotype
Pregnancy
Psychiatry
Radiological weapon
Radiology
Respiratory distress
Subdural hemorrhage
Surgery