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Nonprogressive Mobile Dystonia in MTFMT‐Related Mitochondrial Disease

• Authors : Kallol Kumar Set; Karl De Dios

Subjects: 03 medical and health sciences; 0302 clinical medicine

• Source: Movement Disorders Clinical Practice. 10:145-147

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Deep Brain Stimulation in a Case of Mitochondrial Disease

• Authors : Daniel Martinez‐Ramirez; Nawaz Hack; Matthew L. Vasquez

Subjects: 2. Zero hunger; 03 medical and health sciences; 0302 clinical medicine

• Source: Movement Disorders Clinical Practice. 3:139-145

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Biallelic Loss‐of‐Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh‐Like Syndrome to Isolated Optic Atrophy

• Authors : Francesca Magrinelli; Elisa Calì; Vinícius Lopes Braga ...

Subjects: NDUFA12; Clinical Biochemistry; Gene

• Source: Mov Disord Clin PractMagrinelli, F, Cali, E, Braga, V L, Yis, U, Tomoum, H, Shamseldin, H, Raiman, J, Kernstock, C, Rezende Filho, F M, Povoas Barsottini, O G, Taylor, R W, Ostergaard, E, Tamim,

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Nonprogressive Mobile Dystonia in MTFMT-Related Mitochondrial Disease.

• Authors : Kumar, Kallol; De Dios, Karl

Subjects: DYSTONIA; MITOCHONDRIA; MOVEMENT disorders

• Source: Movement Disorders Clinical Practice; Jan2023, Vol. 10 Issue 1, p145-147, 3p

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Deep Brain Stimulation in a Case of Mitochondrial Disease.

• Authors : Martinez‐Ramirez, Daniel; Hack, Nawaz; Vasquez, Matthew L.

Subjects: MITOCHONDRIAL pathology; DEEP brain stimulation; BRAIN stimulation

• Source: Movement Disorders Clinical Practice; Mar2016, Vol. 3 Issue 2, p139-145, 7p

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Generalized Dystonia as a Cardinal Manifestation of Combined Oxidative Phosphorylation Deficiency 1.

• Authors : Nayan, Aditya¹ (AUTHOR); Mehta, Shivangi² (AUTHOR); Chakravarty, Kamalesh¹ (AUTHOR)

• Source: Movement Disorders Clinical Practice. Jun2024, Vol. 11 Issue 6, p742-745. 4p.

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Acute Ophthalmoplegia with Wernicke‐Like MRI Pattern in a Patient with HPDL‐Related Disorder.

• Authors : Sartorelli, Jacopo¹ (AUTHOR); Longo, Daniela² (AUTHOR); Travaglini, Lorena³ (AUTHOR)

• Source: Movement Disorders Clinical Practice. Sep2024, Vol. 11 Issue 9, p1160-1162. 3p.

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Expanding the Phenotypic Variability of PMPCA‐Related Ataxia.

• Authors : Sanesteban‐Beceiro, Esteban¹ (AUTHOR) ; Fenollar‐Cortés, María² (AUTHOR); Herrero‐Forte, Clara² (AUTHOR)

• Source: Movement Disorders Clinical Practice. Jul2024, Vol. 11 Issue 7, p894-896. 3p.

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Biallelic Variants in COQ4 Cause Childhood‐Onset Pure Hereditary Spastic Paraplegia.

• Authors : Schierbaum, Luca¹ (AUTHOR); Quiroz, Vicente¹ (AUTHOR); Tam, Amy¹ (AUTHOR)

• Source: Movement Disorders Clinical Practice. Dec2024, Vol. 11 Issue 12, p1620-1624. 5p.

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Biallelic Loss‐of‐Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh‐Like Syndrome to Isolated Optic Atrophy.

• Authors : Magrinelli, Francesca; Cali, Elisa; Braga, Vinícius Lopes

Subjects: MOVEMENT disorders; ATROPHY; GENETIC databases

• Source: Movement Disorders Clinical Practice; Feb2022, Vol. 9 Issue 2, p218-228, 11p

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