• 548 Citations
  • 14 h-Index
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Fingerprint Dive into the research topics where K. Komlósi is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 17 Similar Profiles
Mutation Medicine & Life Sciences
Carnitine Medicine & Life Sciences
Genes Medicine & Life Sciences
Mitochondrial DNA Medicine & Life Sciences
Esters Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Alleles Medicine & Life Sciences
Hearing Loss Medicine & Life Sciences

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Research Output 2001 2019

  • 548 Citations
  • 14 h-Index
  • 55 Article
  • 2 Chapter
  • 2 Comment/debate

Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutation

Gucev, Z., Tasic, V., Bogevska, I., Laban, N., Saveski, A., Polenakovic, M., Plaseska-Karanfilska, D., Komlósi, K., Winter, J., Schweiger, S., Nishimura, G., Spranger, J. & Bartsch, O., jan. 1 2019, (Accepted/In press) In : European Journal of Medical Genetics.

Research output: Article

Neurogenic Arthropathy
Hereditary Sensory and Autonomic Neuropathies
Heterotopic Ossification

The Clinical and Molecular Spectrum of GM1 Gangliosidosis

Arash-Kaps, L., Komlosi, K., Seegräber, M., Diederich, S., Paschke, E., Amraoui, Y., Beblo, S., Dieckmann, A., Smitka, M. & Hennermann, J. B., dec. 2019, In : Journal of Pediatrics. 215, p. 152-157.e3

Research output: Article

GM1 Gangliosidosis
Dystonic Disorders
Muscle Spasticity
1 Citation (Scopus)
Hearing Loss