DOI:
10.1055/s-00000041
Neuropediatrics
Issue 04 ·
Volume 52 ·
August 2021
DOI: 10.1055/s-011-51378
Review Article
Original Article
274
Gburek-Augustat, Janina;
Schoene-Bake, Jan-Christoph;
Bültmann, Eva;
Haack, Tobias;
Buchert, Rebecca;
Synofzik, Matthis;
Biskup, Saskia;
Feuerhake, Friedrich;
Sorge, Ina;
Hartmann, Hans:
Pitfalls in Genetic Diagnostics: Why Phenotyping is Essential
302
Kraoua, Ichraf;
Bouyacoub, Yosra;
Drissi, Cyrine;
Chargui, Mariem;
Rebai, Ibtihel;
Chebil, Ahmed;
Klaa, Hédia;
Benrhouma, Hanene;
Hassen, Aida;
Gouider-Khouja, Neziha;
Abdelhak, Sonia;
Boespflug-Tanguy, Odile;
Youssef-Turki, Ilhem Ben;
Dorboz, Imen:
Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review
Short Communication
337
Yazbeck, Elise;
Maurey, Hélène;
Leroy, Carole;
Horellou, Philippe;
Napuri, Silvia;
Lali, Mohammed;
Adam, Clovis;
Husson, Beatrice;
Sevin, Caroline;
Deiva, Kumaran:
Progressive Leukodystrophy-Like Demyelinating Syndromes with MOG-Antibodies in Children: A Rare Under-Recognized Phenotype
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