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Parman

Showing results (121-130 of 316) with videos related to

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Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|October 12, 2011
Increased complement consumption in MuSK-antibody-positive myasthenia gravis patientsErdem Tüzün, Vuslat Yılmaz, Yeşim Parman, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 20, 2023
A novel homozygous loss-of-function variant in SOD1 causing progressive spastic tetraplegia and axial hypotoniaArman Çakar, Emre Pekbilir, Serdar Ceylaner, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|July 25, 2019
Assessment of patients with hereditary transthyretin amyloidosis - understanding the impact of management and disease progressionIsabel Conceição, Teresa Coelho, Claudio Rapezzi, et al.
American Journal of Hypertension|May 13, 2016
Potential Errors and Omissions Related to the Analysis and Conclusions Reported in Cuspidi C, et al., AJH 2014; 27(2):146-156Kathryn A Kaiser, Mariel A Parman, Eric Kim, et al.
Noro Psikiyatri Arsivi|March 23, 2022
Lumbar Spinal Stenosis: A Rare Presentation of Hereditary Transthyretin AmyloidosisArman Çakar, Murat Mert Atmaca, Dilcan Kotan, et al.
Muscle & Nerve|September 24, 2022
Disease activity in chronic inflammatory demyelinating polyneuropathy: A comparative study of clinical and skin biopsy markersAyşe Nur Özdağ Acarli, Gökçen Ünverengil, Nermin Görkem Şirin, et al.
Neurogenetics|November 2, 2019
The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotypeAyşe Candayan, Gulshan Yunisova, Arman Çakar, et al.
Hormone Research|January 1, 1986
The antidiabetic activity of aloes: preliminary clinical and experimental observationsN Ghannam, M Kingston, I A Al-Meshaal, et al.
Mitochondrion|March 2, 2026
Late-onset TK2 deficiency in adults: Long-term clinical outcomes of deoxynucleoside therapyHacer Durmus, Asuman Gedikbaşı, Serdar Ceylaner, et al.
European Journal of Immunology|September 17, 2024
In vitro modulation of T cells in myasthenia gravis by low-dose IL-2Merve Çebi, Arman Çakar, Hacer Durmuş, et al.
Pageof 32

Showing results (121-130 of 316) with videos related to

Sort By:
Pageof 32
Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|October 12, 2011
Increased complement consumption in MuSK-antibody-positive myasthenia gravis patientsErdem Tüzün, Vuslat Yılmaz, Yeşim Parman, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 20, 2023
A novel homozygous loss-of-function variant in SOD1 causing progressive spastic tetraplegia and axial hypotoniaArman Çakar, Emre Pekbilir, Serdar Ceylaner, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|July 25, 2019
Assessment of patients with hereditary transthyretin amyloidosis - understanding the impact of management and disease progressionIsabel Conceição, Teresa Coelho, Claudio Rapezzi, et al.
American Journal of Hypertension|May 13, 2016
Potential Errors and Omissions Related to the Analysis and Conclusions Reported in Cuspidi C, et al., AJH 2014; 27(2):146-156Kathryn A Kaiser, Mariel A Parman, Eric Kim, et al.
Noro Psikiyatri Arsivi|March 23, 2022
Lumbar Spinal Stenosis: A Rare Presentation of Hereditary Transthyretin AmyloidosisArman Çakar, Murat Mert Atmaca, Dilcan Kotan, et al.
Muscle & Nerve|September 24, 2022
Disease activity in chronic inflammatory demyelinating polyneuropathy: A comparative study of clinical and skin biopsy markersAyşe Nur Özdağ Acarli, Gökçen Ünverengil, Nermin Görkem Şirin, et al.
Neurogenetics|November 2, 2019
The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotypeAyşe Candayan, Gulshan Yunisova, Arman Çakar, et al.
Hormone Research|January 1, 1986
The antidiabetic activity of aloes: preliminary clinical and experimental observationsN Ghannam, M Kingston, I A Al-Meshaal, et al.
Mitochondrion|March 2, 2026
Late-onset TK2 deficiency in adults: Long-term clinical outcomes of deoxynucleoside therapyHacer Durmus, Asuman Gedikbaşı, Serdar Ceylaner, et al.
European Journal of Immunology|September 17, 2024
In vitro modulation of T cells in myasthenia gravis by low-dose IL-2Merve Çebi, Arman Çakar, Hacer Durmuş, et al.
Pageof 32