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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 syndrome
Erdal 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 orientation
Oscar 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 cases
Nazan 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 literature
Mehmet 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 syndrome
Nicholas 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 function
Søren 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 TUBB3
Nicholas 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 dysfunction
Sofia Zoullas, Dayna Morel, Faraz Zafeer, et al.
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of 24
Search research articles
Search
Showing results (81-90 of 235) with videos related to
Sort By:
Page
of 24
Pediatrics International : Official Journal of the Japan Pediatric Society
|
September 30, 2005
Characteristics of hyperthermia and its complications in patients with Prader Willi syndrome
Erdal 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 orientation
Oscar 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 cases
Nazan 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 literature
Mehmet 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 syndrome
Nicholas 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 function
Søren 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 TUBB3
Nicholas 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 dysfunction
Sofia Zoullas, Dayna Morel, Faraz Zafeer, et al.
Page
of 24