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