Mitochondrial membrane protein-associated neurodegeneration (MPAN): Two phenotypes—dystonia and spastic paraparesis

Mitochondrial membrane protein-associated neurodegeneration (MPAN): Two phenotypes—dystonia and spastic paraparesis

Bibliographic Details
Main Authors:	Sruthi Kola, Sai S L. Meka, Syed T Fathima, Abdul Wahed, Rukmini M Kandadai, Rupam Borgohain
Format:	Article
Language:	English
Published:	Wolters Kluwer Medknow Publications 2022-01-01
Series:	Annals of Indian Academy of Neurology
Online Access:	http://www.annalsofian.org/article.asp?issn=0972-2327;year=2022;volume=25;issue=6;spage=1200;epage=1202;aulast=Kola

Similar Items

Dystonia deafness syndrome: A rare deep brain stimulation responsive dystonia
by: Sruthi Kola, et al.
Published: (2023-01-01)

Constant current versus constant voltage DBS stimulators—Changing trend
by: Rukmini M Kandadai, et al.
Published: (2023-01-01)

Guidelines for the use of botulinum toxin in movement disorders and spasticity
by: Jabeen Afshan, et al.
Published: (2011-01-01)

Study of Impact of Stereotactic parameters on Microelectrode recording in Parkinson’s disease patients who underwent Subthalamic nucleus Deep brain stimulation
by: Sruthi Kola, et al.
Published: (2023-01-01)

Changes in optimal stimulation frequency with time for gait disturbances in patients with PD after STN-DBS—A longitudinal study
by: Sruthi Kola, et al.
Published: (2023-01-01)

Aceruloplasminemia with novel mutation, with IgG4 related pachymeningitis – occam's razor or hickam's dictum?
by: Sai D Yaranagula, et al.
Published: (2023-01-01)

Effect of medication and deep brain stimulation on gait in Parkinson's disease and its quantitative analysis using Mobishoe – A comparative study
by: Sai Sri Lakshmi Meka, et al.
Published: (2023-01-01)

Identification of Autophagy as a Functional Target Suitable for the Pharmacological Treatment of Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN) In Vitro
by: Enrica Zanuttigh, et al.
Published: (2023-01-01)

Tropical spastic paraparesis-like illness in an HIV-Infected child
by: Sonu Antony, et al.
Published: (2023-01-01)

The coexistence of multiple sclerosis and hereditary spastic paraparesis in a patient
by: Işıl Yazıcı, et al.
Published: (2013-06-01)

Delayed peri-lead intracerebral hemorrhage months after deep brain stimulation: A series of two patients
by: Sai Deepak Yaranagula, et al.
Published: (2024-01-01)

Early-Onset HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis
by: Alvaro Schwalb, et al.
Published: (2020-06-01)

Hereditary Spastic Paraparesis with Thin Corpus Callosum: Characteristic MRI Findings
by: Eser S Sanverdi, et al.
Published: (2011-12-01)

Hereditary Spastic Paraparesis with Thin Corpus Callosum: Characteristic MRI Findings
by: Eser S Sanverdi, et al.
Published: (2011-12-01)

A Novel Deletion Mutation of Exon 2 of the C19orf12 Gene in an Omani Family with Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN)
by: Nabil Al Macki, et al.
Published: (2017-01-01)

A rare case of the complex phenotype of hereditary spastic paraparesis due to a mutation in a novel gene variant
by: B Jude Antonieo Raja, et al.
Published: (2022-01-01)

Plasma proteome analysis in HTLV-1-associated myelopathy/tropical spastic paraparesis.
by: Kirk, P, et al.
Published: (2011)

A rare case of adult-onset spastic paraparesis associated with Klinefelter syndrome
by: Louise Adams, et al.
Published: (2024-01-01)

Health service experiences among adults with hereditary spastic paraparesis or neurofibromatosis type 1
by: Krister W. Fjermestad, et al.
Published: (2020-10-01)

Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement
by: Min-Yu Lan, et al.
Published: (2022-09-01)

The pathogenesis of tropical spastic paraparesis/human T-cell leukemia type I-associated myelopathy
by: Casseb J., et al.
Published: (2000-01-01)

The Central Effects of Botulinum Toxin in Dystonia and Spasticity
by: Pavel Hok, et al.
Published: (2021-02-01)

Enzymatic amplification of exogenous and endogenous retroviral sequences from DNA of patients with tropical spastic paraparesis.
by: Bangham, C, et al.
Published: (1988)

Disseminated cavernous malformations due to KRIT1 gene mutation causing seizure and spastic paraparesis
by: Saranya B Gomathy, et al.
Published: (2024-01-01)

The Relevance of HTLV-1-associated Myelopathy/Tropical Spastic Paraparesis in Iran: A Review Study
by: Masoud Keikha, et al.
Published: (2019-06-01)

Basilar impression associated with impacted cisterna magna, spastic paraparesis and distress of balance: case report
by: José Alberto Gonçalves da Silva, et al.
Published: (2006-09-01)

Impact of fractures and orthopedic surgeries in patients with HTLV-1 associated myelopathy/tropical spastic paraparesis
by: Pablo Julca-Copello, et al.
Published: (2020-09-01)

RNASEH2B pathogenic mutation presenting with pure, Apparently Non-Progressive hereditary spastic paraparesis
by: Ayush Agarwal, et al.
Published: (2023-01-01)

Impaired flexibility in patients with tropical spastic paraparesis/HTLV-associated myelopathy: evaluation via pendulum fleximeter
by: Caroline Landim, et al.
Published: (2023-03-01)

The Barriers of Coping with HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis: A Content Analysis Study
by: Malihe Davoudi, et al.
Published: (2023-10-01)

Oculodentodigital Dysplasia Presenting as Spastic Paraparesis: The First Genetically Confirmed Korean Case and a Literature Review
by: Kye Won Park, et al.
Published: (2017-09-01)

Syringohydromyelia or HTLV-I-associated myelopathy/tropical spastic paraparesis: a diagnostic challenge (case report)
by: ABELARDO DE QUEIROZ-CAMPOS ARAÚJO, et al.
Published: (1999-06-01)

Screening for prolonged incubation of HTLV-I infection in British and Jamaican relatives of British patients with tropical spastic paraparesis.
by: Cruickshank, J, et al.
Published: (1990)

Hereditary spastic paraparesis due to SPG5/CYP7B1 mutation with potential therapeutic implications
by: P. Pérez-Torre, et al.
Published: (2023-11-01)

Pregnancy complicated by HTLV‐1‐associated myelopathy/tropical spastic paraparesis (HAM/TSP): a case report
by: Hiroshi Mori, et al.
Published: (2021-07-01)

An unusual cause for cauda equina and spastic paraparesis: Two cases of brucellar arachnoiditis without spondylodiscitis or constitutional symptoms
by: Deepak Menon, et al.
Published: (2022-01-01)

Adult-onset Leigh′s disease: A rare entity
by: Shaik Afshan Jabeen, et al.
Published: (2016-01-01)

From cirrhosis to paraparesis
by: Ioan-Cristian Lupescu, et al.
Published: (2019-12-01)

Neurodegeneration with progressive dystonia: Juvenile-onset Tay–Sachs disease
by: Jasmine Kaur, et al.
Published: (2022-01-01)

Iliopsoas Muscle Weakness as a Key Diagnostic Marker in HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis (HAM/TSP)
by: Eiji Matsuura, et al.
Published: (2023-04-01)