Name and surname:
|
MUDr. Patrícia Balážová
|
Document type:
|
Research/art/teacher profile of a person
|
The name of the university:
|
Comenius University Bratislava
|
The seat of the university:
|
Šafárikovo námestie 6, 818 06 Bratislava
|
III.a - Occupation-position | III.b - Institution | III.c - Duration |
---|---|---|
doctor | National Institute of Children’s Diseases | 2018 - until now |
a teaching assistant | Commenius University, Faculty of Medicine | 2018 - until now |
IV.a - Activity description, course name, other | IV.b - Name of the institution | IV.c - Year |
---|---|---|
Electromyography Course | The University Hospital Brno | 2023 |
Expert Masterclass in Limb Girdle Muscular Dystrophy | TREAT-NMD Neuromuscular Network | 2023 |
V.5.a - Name of the course | V.5.b - Study programme | V.5.c - Degree | V.5.d - Field of study |
---|---|---|---|
Pediatric Neurology | General Medicine | II. | Pediatrics |
Aitken F., Stanescu I., Balážová P. et al.: A novel rapamycin cream formulation improves facial angiofibromas associated with tuberous sclerosis complex: a double-blind randomized placebo-controlled trial, British Journal of Dermatology, Volume 189, Issue 5, November 2023, Pages 520–530 (IF= 10,3 Q1)
Balážová P, Viestová K, Kolníková M. Dystrophinopathies. Ces-slov Pediat. 2022;77(4):198-205.
Balážová P., Viestová K., Kolníková M. LAMA2-associated muscular dystrophies - clinical and radiological features (case report). Neurológia. 2023, 18(1), 51-55. ISSN 1336-8621.
Balážová P., Viestová K., Kolníková M. Congenital myopathy associated with RYR1 gene mutation (case report). Neurológia pre prax. 2021, 22(3), 202-205. ISSN 1335-9592.
Balážová P., Kolníková M.: Spinal muscular atrophy diagnostic options and treatment. Pediatria pre prax. 2019, 20(6), 239-242.
Aitken F., Stanescu I., Balážová P. et al.: A novel rapamycin cream formulation improves facial angiofibromas associated with tuberous sclerosis complex: a double-blind randomized placebo-controlled trial, British Journal of Dermatology, Volume 189, Issue 5, November 2023, Pages 520–530. (IF= 10,3 Q1)
Balážová P, Viestová K, Kolníková M. Dystrophinopathies. Ces-slov Pediat. 2022;77(4):198-205.
Balážová P., Viestová K., Kolníková M. LAMA2-associated muscular dystrophies - clinical and radiological features (case report). Neurológia. 2023, 18(1), 51-55. ISSN 1336-8621.
Balážová P., Viestová K., Kolníková M. Congenital myopathy associated with RYR1 gene mutation (case report). Neurológia pre prax. 2021, 22(3), 202-205. ISSN 1335-9592.
Balážová P., Kolníková M.: Spinal muscular atrophy diagnostic options and treatment. Pediatria pre prax. 2019, 20(6), 239-242.