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Meliha Tan

Showing results (21-30 of 36) with videos related to

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Case Reports in Neurology|September 18, 2010
Woman with Sickle Cell Disease with Current Sigmoid Sinus Thrombosis and History of Inadequate Warfarin Use during a Past Thrombotic EventAsuman Celikbilek, Mehmet Celikbilek, Alper Bozkurt, et al.
The International Journal of Neuroscience|July 31, 2003
Differential contributions of right and left brains to paw skill in right- and left-pawed female ratsDerya Deniz Elalmis, Kerem Tuncay Ozgünen, Seçil Binokay, et al.
The International Journal of Neuroscience|January 8, 2005
Personality, depression, and anxiety as risk factors for chronic migraineBaşak Karakurum, Ozlem Soylu, Mehmet Karataş, et al.
The International Journal of Neuroscience|February 27, 2008
"Unertan syndrome" in two Turkish families in relation to devolution and emergence of Homo erectus: neurological examination, MRI, and PET scansUner Tan, Sadrettin Pençe, Mustafa Yilmaz, et al.
The International Journal of Neuroscience|October 15, 2005
Silent cerebral infarct in patients with mitral valve prolapseBaşak Karakurum, Semra Topçu, Tulin Yildirim, et al.
Noro Psikiyatri Arsivi|April 1, 2017
If Neurologists Establish The Diagnosis of Primary Sjogren's Syndrome?Sibel Karaca, Emine Duygu Ersözlü Bozkirli, Başak Karakurum Göksel, et al.
The International Journal of Neuroscience|November 29, 2007
Unertan syndrome: a case series demonstrating human devolutionUner Tan, Sibel Karaca, Meliha Tan, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|April 28, 2015
A Rare Complication Developing After Hematopoietic Stem Cell Transplantation: Wernicke's EncephalopathySoner Solmaz, Çiğdem Gereklioğlu, Meliha Tan, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 11, 2008
Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humansTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 12, 2008
Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotionTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

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Pageof 4
Case Reports in Neurology|September 18, 2010
Woman with Sickle Cell Disease with Current Sigmoid Sinus Thrombosis and History of Inadequate Warfarin Use during a Past Thrombotic EventAsuman Celikbilek, Mehmet Celikbilek, Alper Bozkurt, et al.
The International Journal of Neuroscience|July 31, 2003
Differential contributions of right and left brains to paw skill in right- and left-pawed female ratsDerya Deniz Elalmis, Kerem Tuncay Ozgünen, Seçil Binokay, et al.
The International Journal of Neuroscience|January 8, 2005
Personality, depression, and anxiety as risk factors for chronic migraineBaşak Karakurum, Ozlem Soylu, Mehmet Karataş, et al.
The International Journal of Neuroscience|February 27, 2008
"Unertan syndrome" in two Turkish families in relation to devolution and emergence of Homo erectus: neurological examination, MRI, and PET scansUner Tan, Sadrettin Pençe, Mustafa Yilmaz, et al.
The International Journal of Neuroscience|October 15, 2005
Silent cerebral infarct in patients with mitral valve prolapseBaşak Karakurum, Semra Topçu, Tulin Yildirim, et al.
Noro Psikiyatri Arsivi|April 1, 2017
If Neurologists Establish The Diagnosis of Primary Sjogren's Syndrome?Sibel Karaca, Emine Duygu Ersözlü Bozkirli, Başak Karakurum Göksel, et al.
The International Journal of Neuroscience|November 29, 2007
Unertan syndrome: a case series demonstrating human devolutionUner Tan, Sibel Karaca, Meliha Tan, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|April 28, 2015
A Rare Complication Developing After Hematopoietic Stem Cell Transplantation: Wernicke's EncephalopathySoner Solmaz, Çiğdem Gereklioğlu, Meliha Tan, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 11, 2008
Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humansTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 12, 2008
Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotionTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
Pageof 4