Articles by author - Tatána Maríková

Mid-aortic syndrome with renovascular hypertension and multisystem involvement in a girl with familiar neurofibromatosis von Recklinghausen type 1.

Petrak B, Bendova S, Seeman T, Klein T, Lisy J, Zatrapa T, Marikova T.

Case Reports 2007; 28(6): 734-738 PubMed PMID: 18063929  Keywords:  Aorta, Abdominal:abnormalities, Aortic Diseases:complications, Child, Child, Preschool, Constriction, Pathologic, Female, Glioma:complications, Humans, Hypertension, Renovascular:complications, Hypertrophy, Left Ventricular:complications, Mutation, Neurof.    Citation

OBJECTIVES: Neurofibromatosis von Recklinghausen type 1 (NF1) is an autosomal dominant neurocutaneous disorder affecting one in 3 000-4 00.....

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First cases in the Czech Republic of the Hallervorden-Spatz disease resulting from mutation in the pantothenate kinase 2 gene.

Zumrová A, Krepelová A, Kyncl M, Maríková T, Prosková M, Cíbochová R, Sebronová V, Komárek V.

Case Reports 2005; 26(3): 213-218 PubMed PMID: 15990724  Keywords:  Adolescent, Adult, Basal Ganglia:pathology, Calcinosis:genetics, Child, Child, Preschool, Czech Republic, Diagnosis, Differential, Dyskinesias:genetics, Family Health, Female, Humans, Magnetic Resonance Imaging, Male, Mutation, Pantothenate Kinase-Associa.    Citation

: Hallervorden-Spatz disease (HSD) was and is known as a rare disorder primarily characterized by progressive extrapyramidal dysfunction a.....

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