Výsledky vyhledávání - "Zarrouk Mahjoub S"

Akademický článek

Mitochondrial multiorgan disorder syndrome score generated from definite mitochondrial disorders

Publikováno v: Neuropsychiatric Disease and Treatment, Vol Volume 13, Pp 2569-2579 (2017)

Josef Finsterer,1 Sinda Zarrouk-Mahjoub2 1Municipal Hospital Rudolfstiftung, Vienna, Austria; 2Genomics Platform, Pasteur Institute of Tunis, Tunis, Tunisia Objectives: Mitochondrial disorders (MIDs) frequently present as mitochondrial multiorgan dis

Externí odkaz: https://doaj.org/article/a65a2776e129472993cefb9ee89c3090

Zobrazit plný text záznamu

Akademický článek

Psychological morbidity in Leber’s hereditary optic neuropathy depends on phenotypic, social, economic, and genetic factors

Autor: Finsterer J, Zarrouk-Mahjoub S

Publikováno v: Clinical Ophthalmology, Vol Volume 11, Pp 959-962 (2017)

Josef Finsterer,1 Sinda Zarrouk-Mahjoub2 1Krankenanstalt Rudolfstiftung, Vienna, Austria; 2University of Tunis El Manar, Genomics Platform, Pasteur Institute of Tunis, Tunis, Tunisia We have read with interest the article by Garcia et al1 about the e

Externí odkaz: https://doaj.org/article/f1ddd2e8fdfa4501a747714b6d7d85f7

Zobrazit plný text záznamu

Akademický článek

Pro- and anti-inflammatory cytokines in post-infarction left ventricular remodeling

Autor: Zarrouk-Mahjoub, S., Zaghdoudi, M., Amira, Z., Chebi, H., Khabouchi, N., Finsterer, J., Mechmeche, R., Ghazouani, E.

Publikováno v: In International Journal of Cardiology 15 October 2016 221:632-636

Zobrazit plný text záznamu

Akademický článek

Leber’s hereditary optic neuropathy is multiorgan not mono-organ

Autor: Finsterer J, Zarrouk-Mahjoub S

Publikováno v: Clinical Ophthalmology, Vol Volume 10, Pp 2187-2190 (2016)

Josef Finsterer,1 Sinda Zarrouk-Mahjoub2 1Krankenanstalt Rudolfstiftung, Vienna, Austria; 2Genomics Platform, Pasteur Institute of Tunis, Tunisia Abstract: Leber’s hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disorder

Externí odkaz: https://doaj.org/article/541f04ebf2cf41f1b29bff2f274ea315

Zobrazit plný text záznamu

Akademický článek

Detection of the mutation may guide treatment of heart and muscle in Duchenne muscular dystrophy

Autor: Finsterer J, Zarrouk-Mahjoub S

Publikováno v: International Medical Case Reports Journal, Vol 2016, Iss Issue 1, Pp 55-56 (2016)

Josef Finsterer,1 Sinda Zarrouk-Mahjoub21Krankenanstalt Rudolfstiftung, Vienna, Austria; 2Genomics Platform, Pasteur Institute of Tunis, Tunis, Tunisia We read with great interest the article, by Kono et al, about a 32-year-old male with Duchenne mus

Externí odkaz: https://doaj.org/article/d60c25f79a94416bb12965f41a47c64a

Zobrazit plný text záznamu