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NTRK1 gene-related congenital insensitivity to pain with anhidrosis: a nationwide multicenter retrospective study.
Echaniz-Laguna, Andoni; Altuzarra, Cecilia; Verloes, Alain; De La Banda, Marta Gomez Garcia; Quijano-Roy, Susana; Tudorache, Raluca Anca; Jaxybayeva, Altynshash; Myrzaliyeva, Bakhytkul; Tazir, Meriem; Vallat, Jean-Michel; Francou, Bruno; Urtizberea, Jon Andoni.
Afiliação
  • Echaniz-Laguna A; Neurology Department, APHP, CHU de Bicêtre, Le Kremlin-Bicêtre, 78 rue du Général Leclerc, 94276, Kremlin-Bicêtre Cedex, France. Andoni.echaniz-laguna@aphp.fr.
  • Altuzarra C; French National Reference Center for Rare Neuropathies (NNERF), 94276, Le Kremlin-Bicêtre, France. Andoni.echaniz-laguna@aphp.fr.
  • Verloes A; INSERM U1195, Paris-Saclay University, 94276, Le Kremlin-Bicêtre, France. Andoni.echaniz-laguna@aphp.fr.
  • De La Banda MGG; Pediatrics Department, Besançon University Hospital, Besançon, France.
  • Quijano-Roy S; Genetics Department, APHP, Robert Debré Hospital, Paris, France.
  • Tudorache RA; Pediatrics Department, Garches University Hospital, Garches, France.
  • Jaxybayeva A; Pediatrics Department, Garches University Hospital, Garches, France.
  • Myrzaliyeva B; Pediatrics Department, Garches University Hospital, Garches, France.
  • Tazir M; Pediatric Neurology Clinic, Obregia Hospital, Bucharest, Romania.
  • Vallat JM; Astana Medical University, Nur-sultan, Kazakhstan.
  • Francou B; Kazakh-Turkish International University, Turkestan, Kazakhstan.
  • Urtizberea JA; Neurology Department, Children's Hospital, Almaty, Kazakhstan.
Neurogenetics ; 22(4): 333-341, 2021 10.
Article em En | MEDLINE | ID: mdl-34405299

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor / Receptor trkA / Hipo-Hidrose / Mutação Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor / Receptor trkA / Hipo-Hidrose / Mutação Idioma: En Ano de publicação: 2021 Tipo de documento: Article