SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Neurologische Klinik und Poliklinik am Universitätsklinikum Würzburg

Description of facility

Director / Spokesperson
Prof. Dr. J. Volkmann
Information
Care facility for adults and children
Description
Die Neurologie hat sich in den letzten 20 Jahren von einem diagnostischen zu einem therapeutischen Fach gewandelt. Schlaganfall, multiple Sklerose, Parkinson-Krankheit, Epilepsien, Nerven- und Muskelerkrankungen sind heute vielfältig behandelbar. Die neurologische Klinik und Poliklinik am Universitätsklinikum Würzburg bietet Diagnostik und Therapie nach modernsten Standards auf dem gesamten Gebiet der Neurologie an.

In zahlreichen Spezialsprechstunden sowie im Rahmen konsiliarischer Untersuchungen werden jährlich fast 11 000 Patientinnen und Patienten behandelt. 3400 werden stationär aufgenommen, davon über 500 intensivmedizinisch. Bei einem Großteil der stationären Aufnahmen handelt es sich um Notfälle, die in der neurologisch-neurochirurgischen Notaufnahme erstversorgt werden. Die Klinik verfügt über 86 Planbetten, darunter acht auf der Stroke Unit und zehn auf der klinikeigenen Intensivstation. Gemeinsam mit dem Zentrum für Psychische Gesundheit wird eine neurogerontopsychiatrische Tagesklinik betrieben, in der bis zu 18 Patientinnen und Patienten mit neuropsychiatrischen Störungen wie etwa Morbus Parkinson interdisziplinär behandelt werden können.

In die Klinik integriert sind die Abteilung für Experimentelle Entwicklungsneurobiologie mit Elektronenmikroskopie und das Liquorlabor.

Care provisions

This facility offers the following
  • Diagnostic
  • Therapy

Contact

Sekretariat
0931 20123751
0931 20123946
nl_direktion@ukw.de
Website http://www.neurologie.ukw.de

Address

Josef-Schneider-Straße 2
97080 Würzburg
Hauptareal des Universitätsklinikums, Bereich B (Haus B1)

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Mentioned by the following facilities 1

Preview of the assigned diseases 8

Autosomal recessive distal hereditary motor neuropathy Brain inflammatory disease Congenital lethal myopathy, Compton-North type Laminin subunit alpha 2-related congenital muscular dystrophy Progressive hemifacial atrophy Fingerprint body myopathy Muscular channelopathy Isaacs syndrome Spheroid body myopathy Distal hereditary motor neuropathy type 1 Emery-Dreifuss muscular dystrophy Distal myopathy with posterior leg and anterior hand involvement Autosomal dominant congenital benign spinal muscular atrophy Huntington disease Duchenne and Becker muscular dystrophy Rippling muscle disease Spinal atrophy-ophthalmoplegia-pyramidal syndrome Limb-girdle muscular dystrophy Niemann-Pick disease type C, adult neurologic onset Acute disseminated encephalomyelitis Zebra body myopathy Reducing body myopathy Proximal spinal muscular atrophy type 1 Juvenile amyotrophic lateral sclerosis Native American myopathy Corpus callosum agenesis-neuronopathy syndrome Skeletal muscle disease Facioscapulohumeral dystrophy Rigid spine syndrome Oculopharyngeal muscular dystrophy Morvan syndrome Distal hereditary motor neuropathy type 2 Myxofibrosarcoma Hypokalemic periodic paralysis Muscular dystrophy Congenital myopathy Infantile myofibromatosis Parkinson-dementia complex of Guam Progressive supranuclear palsy Juvenile polymyositis Paramyotonia congenita of Von Eulenburg Genetic skeletal muscle disease Distal myopathy with anterior tibial onset Hereditary spastic paraplegia Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Muscle filaminopathy Logopenic progressive aphasia Distal hereditary motor neuropathy type 5 KLHL9-related early-onset distal myopathy Acquired skeletal muscle disease Idiopathic inflammatory myopathy Ullrich congenital muscular dystrophy Frontotemporal dementia Progressive muscular dystrophy Distal anoctaminopathy Metabolic myopathy Congenital muscular dystrophy with integrin alpha-7 deficiency Distal myopathy with early respiratory muscle involvement Neuromuscular junction disease Myotonic dystrophy Autosomal recessive distal myopathy Congenital muscular dystrophy with hyperlaxity Hereditary continuous muscle fiber activity Distal nebulin myopathy Tel Hashomer camptodactyly syndrome Brody myopathy Genetic neuromuscular junction disease Autosomal dominant distal myopathy Lambert-Eaton myasthenic syndrome Acquired neuromuscular junction disease Distal spinal muscular atrophy type 3 Distal hereditary motor neuropathy, Jerash type Classic progressive supranuclear palsy syndrome Non-dystrophic myopathy Distal myotilinopathy Inclusion myopathy X-linked distal spinal muscular atrophy type 3 Vogt-Koyanagi-Harada disease Alpha-crystallinopathy Eosinophilic fasciitis Late-onset distal myopathy, Markesbery-Griggs type Motor neuron disease Synaptic congenital myasthenic syndromes Congenital muscular dystrophy due to LMNA mutation Acquired motor neuron disease Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Miyoshi myopathy Genetic motor neuron disease Cylindrical spirals myopathy Inflammatory myopathy with abundant macrophages Myotonia fluctuans Genetic periodic paralysis Acetazolamide-responsive myotonia Progressive supranuclear palsy-parkinsonism syndrome Myopathy with hexagonally cross-linked tubular arrays Spinal muscular atrophy with respiratory distress type 1 King-Denborough syndrome Autosomal dominant proximal spinal muscular atrophy Myasthenia gravis Progressive supranuclear palsy-pure akinesia with gait freezing syndrome Adult-onset myasthenia gravis Andersen-Tawil syndrome Macrophagic myofasciitis Myofibrillar myopathy Atypical progressive supranuclear palsy syndrome Hereditary inclusion body myopathy type 4 Poliomyelitis Centronuclear myopathy Cluster headache Neuromuscular disease Muscular lipidosis Progressive supranuclear palsy-corticobasal syndrome Juvenile primary lateral sclerosis Muscular glycogenosis Tubular aggregate myopathy Fatal post-viral neurodegenerative disorder Polymyositis Trichinellosis Infantile-onset X-linked spinal muscular atrophy Alveolar rhabdomyosarcoma Inclusion body myopathy with Paget disease of bone and frontotemporal dementia GNE myopathy Distal myopathy, Welander type Guillain-Barré syndrome Juvenile myasthenia gravis Progressive supranuclear palsy-progressive non-fluent aphasia syndrome Proximal myotonic myopathy Nemaline myopathy X-linked myopathy with postural muscle atrophy Tibial muscular dystrophy Bethlem muscular dystrophy X-linked myopathy with excessive autophagy Early-onset autosomal dominant Alzheimer disease Inclusion body myositis Fetal akinesia-cerebral and retinal hemorrhage syndrome Hereditary myopathy with early respiratory failure Infantile-onset ascending hereditary spastic paralysis Intellectual disability-myopathy-short stature-endocrine defect syndrome Myotonic syndrome Sporadic Creutzfeldt-Jakob disease Chronic inflammatory demyelinating polyneuropathy Congenital myasthenic syndromes with glycosylation defect Thomsen and Becker disease Periodic paralysis Autosomal dominant spastic paraplegia type 17 Proximal spinal muscular atrophy Pontocerebellar hypoplasia type 1 Overlap myositis Muscular tumor Bulbospinal muscular atrophy of adult Congenital fibrosis of extraocular muscles CLIPPERS Behavioral variant of frontotemporal dementia Postpoliomyelitis syndrome Laing early-onset distal myopathy Monomelic amyotrophy Rippling muscle disease with myasthenia gravis Generalized bulbospinal muscular atrophy Antisynthetase syndrome CANOMAD syndrome Cyprus facial-neuromusculoskeletal syndrome Autosomal recessive lower motor neuron disease with childhood onset Proximal spinal muscular atrophy type 4 Infectious, fungal or parasitic myopathy Proximal spinal muscular atrophy type 2 Proximal spinal muscular atrophy type 3 Dermatomyositis Bacterial myositis Early-onset myopathy with fatal cardiomyopathy Viral myositis Focal myositis Parasitic myositis Primary lateral sclerosis Opsoclonus-myoclonus syndrome Frontotemporal dementia with motor neuron disease Polyneuropathy associated with IgM monoclonal gammopathy with anti-MAG Progressive non-fluent aphasia Juvenile overlap myositis Semantic dementia Friedreich ataxia Primary progressive aphasia Myosin storage myopathy Griscelli syndrome type 1 Fungal myositis Juvenile idiopathic inflammatory myopathy Myosclerosis Posterior cortical atrophy Niemann-Pick disease type C Multiple sclerosis variant Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy Schilder disease Muscular dystrophy-white matter spongiosis syndrome Amyotrophic lateral sclerosis type 4 Niemann-Pick disease type C, severe perinatal form Young adult-onset distal hereditary motor neuropathy Juvenile dermatomyositis Metabolic myopathy due to lactate transporter defect Spinal muscular atrophy associated with central nervous system anomaly Benign Samaritan congenital myopathy Congenital muscular dystrophy due to dystroglycanopathy Congenital fiber-type disproportion myopathy Lower motor neuron syndrome with late-adult onset Niemann-Pick disease type C, severe early infantile neurologic onset Madras motor neuron disease Autosomal dominant adult-onset proximal spinal muscular atrophy Marburg acute multiple sclerosis Rare neuroinflammatory or neuroimmunological disease Niemann-Pick disease type C, juvenile neurologic onset Baló concentric sclerosis Desmin-related myopathy with Mallory body-like inclusions Alpha-B crystallin-related late-onset myopathy Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Megaconial congenital muscular dystrophy Niemann-Pick disease type C, late infantile neurologic onset Familial hemophagocytic lymphohistiocytosis Neuromyelitis optica spectrum disorder Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Neurogenic scapuloperoneal syndrome, Kaeser type Congenital myopathy, Paradas type Hyperkalemic periodic paralysis Finnish upper limb-onset distal myopathy Immune-mediated necrotizing myopathy Adult-onset distal myopathy due to VCP mutation Rare dystonia Amyotrophic lateral sclerosis Autosomal recessive myogenic arthrogryposis multiplex congenita Cap myopathy Myotonia permanens Amyloidosis Congenital myopathy with cores Riboflavin transporter deficiency Congenital muscular dystrophy Congenital muscular dystrophy type 1B Congenital myasthenic syndrome Oculopharyngodistal myopathy Distal myopathy Vocal cord and pharyngeal distal myopathy Congenital myopathy with excess of thin filaments Desminopathy Postsynaptic congenital myasthenic syndromes Presynaptic congenital myasthenic syndromes Potassium-aggravated myotonia Hereditary myopathy with lactic acidosis due to ISCU deficiency Congenital myotonia Muscular dystrophy, Selcen type Autosomal dominant distal hereditary motor neuropathy Frontotemporal degeneration with dementia Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Thyrotoxic periodic paralysis Rhabdomyosarcoma Steinert myotonic dystrophy Schwartz-Jampel syndrome Idiopathic camptocormia Non-dystrophic myopathy with collagen 6 anomaly Transient neonatal myasthenia gravis Bulbospinal muscular atrophy Bulbospinal muscular atrophy of childhood Intellectual disability-developmental delay-contractures syndrome IgG4-related pachymeningitis Embryonal rhabdomyosarcoma Autosomal dominant childhood-onset proximal spinal muscular atrophy DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy ATTRV30M amyloidosis Pontocerebellar hypoplasia type 2 Frontotemporal dementia, right temporal atrophy variant Encephalitis Arthrogryposis due to muscular dystrophy Distal hereditary motor neuropathy type 7 Idiopathic eosinophilic myositis Kennedy disease

Provided care options 6

# Contact person
1
Spezialambulanz für Bewegungsstörungen
Dr. Chi Wang Ip

0931 20123768
Email
Website
Di ab 8:45 Uhr und Mi ab 11:00 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

2
Sprechstunde für neuromuskuläre Erkrankungen
Prof. Dr. C. Sommer, Prof. Dr. G. Stoll

0931 20123768
Email
Website
Mo ab 8:30 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

3
Spezialambulanz für Motoneuron-Erkrankungen
Dr. D. Zeller

0931 20123768
Email
Website
Di ab 12:30 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

4
Spezialambulanz für Multiple Sklerose und andere entzündliche ZNS-Erkrankungen
Prof. Dr. G. Stoll

0931 20123768
Email
Website
Mo - Fr ab 8:00 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

5
Spezialambulanz für seltene Gedächtnisstörungen
Dr. Jentschke

0931 20123768
Email
Website
Do ab 13:30 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

6
Myasthenie-Sprechstunde
Prof. Dr. G. Stoll

0931 20123768
Email
Website
Mo ab 13:00 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

9.953800749.8007685Neurologische Klinik und Poliklinik am Universitätsklinikum Würzburg
Last updated: 22.05.2023