Neuromyelitis Optica in a Patient from Family with both Myotonic Dystrophy Type 1 and 2.

Rakocevic-Stojanovic, V; Peric, S; Dujmovic, I; Drulovic, J; Pesovic, J; Savic-Pavicevic, D

Neuromyelitis Optica in a Patient from Family with both Myotonic Dystrophy Type 1 and 2.

Rakocevic-Stojanovic, V; Peric, S; Dujmovic, I; Drulovic, J; Pesovic, J; Savic-Pavicevic, D.

Afiliação

Rakocevic-Stojanovic V; Neurology Clinic, Clinical Center of Serbia, School of Medicine, University of Belgrade, Belgrade, Serbia.
Peric S; Neurology Clinic, Clinical Center of Serbia, School of Medicine, University of Belgrade, Belgrade, Serbia.
Dujmovic I; Neurology Clinic, Clinical Center of Serbia, School of Medicine, University of Belgrade, Belgrade, Serbia.
Drulovic J; Neurology Clinic, Clinical Center of Serbia, School of Medicine, University of Belgrade, Belgrade, Serbia.
Pesovic J; Center for Human Molecular Genetics, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Savic-Pavicevic D; Center for Human Molecular Genetics, Faculty of Biology, University of Belgrade, Belgrade, Serbia.

J Neuromuscul Dis ; 4(1): 89-92, 2017.

Article em En | MEDLINE | ID: mdl-28106565

Assuntos

Distrofia Miotônica/complicações; Neuromielite Óptica/complicações; Adolescente; Adulto; Idoso; Família; Feminino; Humanos; Masculino; Pessoa de Meia-Idade; Mutação; Distrofia Miotônica/genética; Miotonina Proteína Quinase/genética; Linhagem; Proteínas de Ligação a RNA/genética; Adulto Jovem

Palavras-chave

Myotonic dystrophy type 1; autoimmune diseases; myotonic dystrophy type 2; neuromyelitis optica

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuromielite Óptica / Distrofia Miotônica Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Neuromuscul Dis Ano de publicação: 2017 Tipo de documento: Article

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