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Ismail Kurt

Showing results (1-10 of 43) with videos related to

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Human Genetics|October 11, 2008
Gene symbol: HMBS. Disease: Porphyria, acute intermittentDana Ulbrichova, Ismail Kurt, Jiri Zeman, et al.
Biological Trace Element Research|August 19, 2009
Chromium, cadmium, and lead levels in urine of children with autism and typically developing controlsOzgür Yorbik, Ismail Kurt, Adnan Haşimi, et al.
Rheumatology International|January 17, 2004
MEFV mutations in familial Mediterranean fever: association of M694V homozygosity with arthritisAbdullah Olgun, Serif Akman, Ismail Kurt, et al.
Clinical Biochemistry|February 4, 2010
Circulating adiponectin levels in post-menopausal women with and without osteoporosisSerkan Tapan, Teoman Dogru, Alper Sonmez, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 30, 2005
A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorptionFaysal Gok, Halil I Aydin, Ismail Kurt, et al.
Nephrology (Carlton, Vic.)|January 4, 2007
Evaluation of renal tubular function in children taking anti-epileptic treatmentBulent Unay, Ridvan Akin, S Umit Sarici, et al.
Journal of Pediatric Ophthalmology and Strabismus|February 28, 2002
Galactokinase deficiency: a case reportIsmail Kurt, Muhittin Serdar, Fatih Mutlu, et al.
Internal Medicine (Tokyo, Japan)|June 19, 2010
Evaluating the validity of serum neopterin and chitotriosidase levels in follow-up brucellosis patientsOmer Coskun, Sukrü Oter, Halil Yaman, et al.
The Turkish Journal of Pediatrics|November 7, 2013
Bullous skin lesions in a jaundiced infant after phototherapy: a case of congenital erythropoietic porphyriaMaşallah Baran, Kayı Eliaçık, Ismail Kurt, et al.
Acta Medica Portuguesa|November 20, 2014
Two cases of the same family with the unusual elevation of CA19-9 levelsMetin Uyanik, Erdim Sertoglu, Muhittin A Serdar, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Human Genetics|October 11, 2008
Gene symbol: HMBS. Disease: Porphyria, acute intermittentDana Ulbrichova, Ismail Kurt, Jiri Zeman, et al.
Biological Trace Element Research|August 19, 2009
Chromium, cadmium, and lead levels in urine of children with autism and typically developing controlsOzgür Yorbik, Ismail Kurt, Adnan Haşimi, et al.
Rheumatology International|January 17, 2004
MEFV mutations in familial Mediterranean fever: association of M694V homozygosity with arthritisAbdullah Olgun, Serif Akman, Ismail Kurt, et al.
Clinical Biochemistry|February 4, 2010
Circulating adiponectin levels in post-menopausal women with and without osteoporosisSerkan Tapan, Teoman Dogru, Alper Sonmez, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 30, 2005
A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorptionFaysal Gok, Halil I Aydin, Ismail Kurt, et al.
Nephrology (Carlton, Vic.)|January 4, 2007
Evaluation of renal tubular function in children taking anti-epileptic treatmentBulent Unay, Ridvan Akin, S Umit Sarici, et al.
Journal of Pediatric Ophthalmology and Strabismus|February 28, 2002
Galactokinase deficiency: a case reportIsmail Kurt, Muhittin Serdar, Fatih Mutlu, et al.
Internal Medicine (Tokyo, Japan)|June 19, 2010
Evaluating the validity of serum neopterin and chitotriosidase levels in follow-up brucellosis patientsOmer Coskun, Sukrü Oter, Halil Yaman, et al.
The Turkish Journal of Pediatrics|November 7, 2013
Bullous skin lesions in a jaundiced infant after phototherapy: a case of congenital erythropoietic porphyriaMaşallah Baran, Kayı Eliaçık, Ismail Kurt, et al.
Acta Medica Portuguesa|November 20, 2014
Two cases of the same family with the unusual elevation of CA19-9 levelsMetin Uyanik, Erdim Sertoglu, Muhittin A Serdar, et al.
Pageof 5