Search Results - "dystonia"

Anti-N-Methyl-d-Aspartate receptor (NMDAR) encephalitis during pregnancy: Clinical analysis of reported cases by Yan-Chao Shi, Xiu-Ju Chen, Hong-Mei Zhang, Zhen Wang, Da-Yong Du

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Profile of pridopidine and its potential in the treatment of Huntington disease: the evidence to date by Squitieri F, de Yebenes JG

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CLINICAL AND ANAMNESTIC CHARACTERISTICS OF PREGNANT WOMEN WITH IODINE DEFICIENCY by Александр Николаевич Мацынин, Андрей Викторович Чурилов, Андрей Васильевич Налетов, Игорь Витальевич Коктышев

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THROMBOPHILIA AS A FACTOR OF ETHIOLOGY AND PATHOGENESYS OF DISORDERS IN THE SYSTEM "WOMAN - FETUS - NEWBORN" by A. Ya. Il'ina, P. V. Shumilov, A. L. Mishchenko, A. S. Barinova, I. Yu. Kokaya, V. N. Kashin, O. S. Pobedinskaya, I. V. Solov'eva, T. S. Kharlamova, A. V. Budancev, E. A. Akhalova

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Burden of illness in aromatic l‐amino acid decarboxylase deficiency by Melissa L. DiBacco, Jordan Hinahara, Thomas F. Goss, Phillip L. Pearl

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Formulation and Clinical Evaluation of Orphenadrine citrate as a Plain Tablet by Abdul Karim F. Jumaa, Alaa A.Abdulrasool, Hikmet A.Al â€" Dujali

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Loss of slc39a14 causes simultaneous manganese hypersensitivity and deficiency in zebrafish by Karin Tuschl, Richard J. White, Chintan Trivedi, Leonardo E. Valdivia, Stephanie Niklaus, Isaac H. Bianco, Chris Dadswell, Ramón González-Méndez, Ian M. Sealy, Stephan C. F. Neuhauss, Corinne Houart, Jason Rihel, Stephen W. Wilson, Elisabeth M. Busch-Nentwich

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Priorities in Movement Disorders Research by Mabel M. Macas, Criscely L. Go, Jose C. Navarro

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P-type ATPases in Health and Disease by Sigrid A. Langhans

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Novel ECHS1 mutations in Leigh syndrome identified by whole-exome sequencing in five Chinese families: case report by Dan Sun, Zhimei Liu, Yongchu Liu, Miaojuan Wu, Fang Fang, Xianbo Deng, Zhisheng Liu, Liang Song, Kei Murayama, Chunhua Zhang, Yuanyuan Zhu

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Self medication in the age of connectivity and its risks - the case report by Andrzej Kościuk, Michał Kos, Justyna Drankowska, Michał Tchórz

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Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports by Hassan Dastsooz, Hamid Nemati, Mohammad Ali Farazi Fard, Majid Fardaei, Mohammad Ali Faghihi

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The Incidence and Clinical Characteristics of the Connective Tissue Dysplasia in Adolescents by Ganna Y. Kalaeva, Оlga I. Khokhlova, Ivan А. Deev, Julia G. Samoilova

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DNM1L-Related Mitochondrial Fission Defects Presenting as Encephalopathy: A Case Report and Literature Review by Xingmiao Liu, Zhongbin Zhang, Dong Li, Meifang Lei, Qing Li, Xiaojun Liu, Peiyuan Zhang

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Complicated Hereditary Spastic Paraplegia Caused by SERAC1 Variants in a Chinese Family by Dandan Yan, Dandan Yan, Shaopei Chen, Fengying Cai, Jianbo Shu, Jianbo Shu, Xiufang Zhi, Xiufang Zhi, Jie Zheng, Jie Zheng, Chunhua Zhang, Dong Li, Chunquan Cai, Chunquan Cai

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Dyke-Davidoff-Masson syndrome: A study of clinicoradiological variability in hemiplegia, hemiatrophy and epilepsy patients by Amita Bhargava, Bharat Bhushan, Gaurav Kasundra, Khichar Shubhakaran, S Pujar Guruprashad, Banakar Basavaraj

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Distinct neonatal hyperammonemia and liver synthesis dysfunction: case report of a severe MEGDHEL syndrome by Ina Kirchberg, Elke Lainka, Andrea Gangfuß, Alma Kuechler, Fabian Baertling, Lea D. Schlieben, Lea D. Schlieben, Dominic Lenz, Eva Tschiedel

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Prenatal diagnosis of fetal glutaric aciduria type 1 with rare compound heterozygous mutations in GCDH gene by Hsiu-Huei Peng, Sheng-Wen Shaw, Kuan-Gen Huang

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Efficacy, tolerability, and safety of lurasidone for acute schizophrenia: A systematic review and network meta‐analysis of phase 3 trials in Japan by Taro Kishi, Tadashi Nosaka, Kenji Sakuma, Makoto Okuya, Nakao Iwata

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Personality and psychopathological profile of patients and botulinum therapy for blepharospasm by Violetta A. Tolmacheva, Polina G. Iuzbashian, Maria D. Samsonova, Dmitry V. Romanov

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