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Person
Person

Person

Alma Osmanovic (1987-)

Neurologin

Name

Alma Osmanovic

Time

1987- (Date of birth and death)

Place

Tuzla (Geburtsort)
Essen (Wirkungsort)
Deutschland

Gender

weiblich

Academic degree

Dr. med. (Univ. Lübeck) (2014)

Profession

Neurologin (characteristic profession)

Variant

A. Osmanovic

Related

Universitätsklinikum Essen

Further information

Habil. Fach Neurologie an der Med. Hochsch. Hannover 2021
Ärztin am Essener Zentrum für seltene Erkrankungen (EZSE) des Universitätsklinikums Essen

Source

Homepage: https://www.uk-essen.de/presse/universitaetsklinikum-essen-wird-ein-modellstandort-fuer-genom-medizin/ (30.10.2023)
Homepage: https://www.zhb.uni-luebeck.de/epubs/ediss1508.pdf (30.10.2023)

Record type

Person

GND-Identifier

1261497589

Record ID

1261497589

Involved in

show all

Risdiplam therapy in adults with 5q-SMA: observational study on motor function and treatment satisfaction

Glial fibrillary acidic protein in cerebrospinal fluid of patients with spinal muscular atrophy

Health-related quality of life in spinal muscular atrophy patients and their caregivers — a prospective, cross-sectional, multi-center analysis

Long-term efficacy and safety of nusinersen in adults with 5q spinal muscular atrophy: a prospective European multinational observational study

Economic evaluation of Motor Neuron Diseases: a nationwide cross-sectional analysis in Germany

An observational cohort study on pulmonary function in adult patients with 5q-spinal muscular atrophy under nusinersen therapy

A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics

Increased chitotriosidase 1 concentration following nusinersen treatment in spinal muscular atrophy

Executive function is inversely correlated with physical function: the cognitive profile of adult Spinal Muscular Atrophy (SMA)

A Nation-Wide, Multi-Center Study on the Quality of Life of ALS Patients in Germany

Heterozygous DHTKD1 variants in two European cohorts of amyotrophic lateral sclerosis patients

Informal Caregiving in Amyotrophic Lateral Sclerosis (ALS): A High Caregiver Burden and Drastic Consequences on Caregivers’ Lives

Translationale Neurogenetik in Motoneuronerkrankungen : Studien zu klinisch-genetischen Schnittstellen und genspezifischen Therapien

Treatment expectations and perception of therapy in adult patients with spinal muscular atrophy receiving nusinersen

Treatment satisfaction in 5q-spinal muscular atrophy under nusinersen therapy

An observational cohort study on impact, dimensions and outcome of perceived fatigue in adult 5q-spinal muscular atrophy patients receiving nusinersen treatment

Costs of illness in amyotrophic lateral sclerosis (ALS): a cross-sectional survey in Germany

SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia

Treatment expectations and patient-reported outcomes of nusinersen therapy in adult spinal muscular atrophy

Impact of comorbidities and co-medication on disease onset and progression in a large German ALS patient group

Cognitive performance of patients with adult 5q-spinal muscular atrophy and with amyotrophic lateral sclerosis

Neurofilament light chain in serum of adolescent and adult SMA patients under treatment with nusinersen

Nusinersen bei spinaler Muskelatrophie : Klinische Anwendbarkeit bei erwachsenen Patienten mit SMA Typ II

Der Transkriptionsfaktor THAP1. Molekulare Schnittstelle zwischen der DYT6- und DYT1-Dystonie
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