Mitochondrial membrane protein-associated neurodegeneration
All Entries 4
Zentrum für mitochondriale Erkrankungen am LMU Klinikum München
Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum LMU Klinikum München
Ziemssenstraße 1
80336 München
089 440057400
089 440057402
Website
Email
- MELAS
- Mitochondrial DNA depletion syndrome
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Pearson syndrome
- MERRF
- Recessive mitochondrial ataxia syndrome
- Barth syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Maternally-inherited diabetes and deafness
- Mitochondrial myopathy
- Mitochondrial neurogastrointestinal encephalomyopathy
- Leber hereditary optic neuropathy
- Kearns-Sayre syndrome
- Coenzyme Q10 deficiency
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Leukodystrophy
- Hereditary spastic paraplegia
- Rare ataxia
- Neurodegeneration with brain iron accumulation
- Neuroferritinopathy
- Mitochondrial disease
- COASY protein-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
- Huntington disease
- Pantothenate kinase-associated neurodegeneration
- Atypical pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration
Institut für Humangenetik am Klinikums rechts der Isar der Technischen Universität München
Klinikum rechts der Isar der Technischen Universität München
Trogerstr. 32
81675 München
089 41406381
089 41406382
Website
Email
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Aceruloplasminemia
- Fatty acid hydroxylase-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- Infantile neuroaxonal dystrophy
- Woodhouse-Sakati syndrome
- Adult-onset dystonia-parkinsonism
- PLA2G6-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Kufor-Rakeb syndrome
- COASY protein-associated neurodegeneration
- Neuroferritinopathy
- Pantothenate kinase-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
Parent facilities 0
Genetic Advices 1
Institut für Humangenetik am Klinikums rechts der Isar der Technischen Universität München
Klinikum rechts der Isar der Technischen Universität München
Trogerstr. 32
81675 München
089 41406381
089 41406382
Website
Email
Care facilities 2
Zentrum für mitochondriale Erkrankungen am LMU Klinikum München
Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum LMU Klinikum München
Ziemssenstraße 1
80336 München
089 440057400
089 440057402
Website
Email
- MELAS
- Mitochondrial DNA depletion syndrome
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Pearson syndrome
- MERRF
- Recessive mitochondrial ataxia syndrome
- Barth syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Maternally-inherited diabetes and deafness
- Mitochondrial myopathy
- Mitochondrial neurogastrointestinal encephalomyopathy
- Leber hereditary optic neuropathy
- Kearns-Sayre syndrome
- Coenzyme Q10 deficiency
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Leukodystrophy
- Hereditary spastic paraplegia
- Rare ataxia
- Neurodegeneration with brain iron accumulation
- Neuroferritinopathy
- Mitochondrial disease
- COASY protein-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
- Huntington disease
- Pantothenate kinase-associated neurodegeneration
- Atypical pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Aceruloplasminemia
- Fatty acid hydroxylase-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- Infantile neuroaxonal dystrophy
- Woodhouse-Sakati syndrome
- Adult-onset dystonia-parkinsonism
- PLA2G6-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Kufor-Rakeb syndrome
- COASY protein-associated neurodegeneration
- Neuroferritinopathy
- Pantothenate kinase-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration