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Mustafa Tekin

Showing results (81-90 of 235) with videos related to

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Pediatrics International : Official Journal of the Japan Pediatric Society|September 30, 2005
Characteristics of hyperthermia and its complications in patients with Prader Willi syndromeErdal Ince, Ergin Ciftçi, Mustafa Tekin, et al.
Journal of Molecular Medicine (Berlin, Germany)|October 4, 2018
Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientationOscar Diaz-Horta, Clemer Abad, Filiz Basak Cengiz, et al.
Molecular Genetics and Metabolism|July 15, 2011
Pyridoxal phosphate-responsive seizures in a patient with cerebral folate deficiency (CFD) and congenital deafness with labyrinthine aplasia, microtia and microdontia (LAMM)Patricia Dill, Jacques Schneider, Peter Weber, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 27, 2014
The effects of passive smoking on the six-minute walk test in obese pediatric casesNazan Kaymaz, Şule Yıldırım, Mustafa Tekin, et al.
Acta Orthopaedica Et Traumatologica Turcica|October 27, 2016
Elastofibroma dorsi: Clinical evaluation of 61 cases and review of the literatureMehmet Ali Deveci, Hilmi Serdar Özbarlas, Kıvılcım Eren Erdoğan, et al.
American Journal of Medical Genetics. Part A|January 11, 2023
Deletion of first noncoding exon in ANKRD11 leads to KBG syndromeNicholas Borja, Mohammad Faraz Zafeer, Jeimy Alfonso Rodriguez, et al.
Journal of Pain Research|June 23, 2016
Does intrauterine tobacco exposure increase the pain perception of newborns?Mustafa Tekin, Şule Yıldırım, Hakan Aylanç, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 12, 2012
Mannan-binding lectin-associated serine protease (MASP)-1 is crucial for lectin pathway activation in human serum, whereas neither MASP-1 nor MASP-3 is required for alternative pathway functionSøren E Degn, Lisbeth Jensen, Annette G Hansen, et al.
Journal of Medical Genetics|December 6, 2024
<i>KIF21A</i>-associated peripheral neuropathy defined by impaired binding with TUBB3Nicholas A Borja, Mohammad Faraz Zafeer, Stephanie Bivona, et al.
American Journal of Medical Genetics. Part A|November 20, 2023
Two novel heterozygous exonic deletions lead to Chanarin-Dorfman syndrome in a patient with congenital ichthyosis, sensorineural hearing loss, and liver dysfunctionSofia Zoullas, Dayna Morel, Faraz Zafeer, et al.
Pageof 24

Showing results (81-90 of 235) with videos related to

Sort By:
Pageof 24
Pediatrics International : Official Journal of the Japan Pediatric Society|September 30, 2005
Characteristics of hyperthermia and its complications in patients with Prader Willi syndromeErdal Ince, Ergin Ciftçi, Mustafa Tekin, et al.
Journal of Molecular Medicine (Berlin, Germany)|October 4, 2018
Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientationOscar Diaz-Horta, Clemer Abad, Filiz Basak Cengiz, et al.
Molecular Genetics and Metabolism|July 15, 2011
Pyridoxal phosphate-responsive seizures in a patient with cerebral folate deficiency (CFD) and congenital deafness with labyrinthine aplasia, microtia and microdontia (LAMM)Patricia Dill, Jacques Schneider, Peter Weber, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 27, 2014
The effects of passive smoking on the six-minute walk test in obese pediatric casesNazan Kaymaz, Şule Yıldırım, Mustafa Tekin, et al.
Acta Orthopaedica Et Traumatologica Turcica|October 27, 2016
Elastofibroma dorsi: Clinical evaluation of 61 cases and review of the literatureMehmet Ali Deveci, Hilmi Serdar Özbarlas, Kıvılcım Eren Erdoğan, et al.
American Journal of Medical Genetics. Part A|January 11, 2023
Deletion of first noncoding exon in ANKRD11 leads to KBG syndromeNicholas Borja, Mohammad Faraz Zafeer, Jeimy Alfonso Rodriguez, et al.
Journal of Pain Research|June 23, 2016
Does intrauterine tobacco exposure increase the pain perception of newborns?Mustafa Tekin, Şule Yıldırım, Hakan Aylanç, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 12, 2012
Mannan-binding lectin-associated serine protease (MASP)-1 is crucial for lectin pathway activation in human serum, whereas neither MASP-1 nor MASP-3 is required for alternative pathway functionSøren E Degn, Lisbeth Jensen, Annette G Hansen, et al.
Journal of Medical Genetics|December 6, 2024
<i>KIF21A</i>-associated peripheral neuropathy defined by impaired binding with TUBB3Nicholas A Borja, Mohammad Faraz Zafeer, Stephanie Bivona, et al.
American Journal of Medical Genetics. Part A|November 20, 2023
Two novel heterozygous exonic deletions lead to Chanarin-Dorfman syndrome in a patient with congenital ichthyosis, sensorineural hearing loss, and liver dysfunctionSofia Zoullas, Dayna Morel, Faraz Zafeer, et al.
Pageof 24