نتائج البحث - "Yener Sahin"

1

Endoscopic Third Ventriculostomy in an Untreated Vein of Galen Malformation Presenting Lately with Acute Obstructive Hydrocephalus

المؤلفون: Adnan Dagcinar, Feyyaz Baltacioglu, Yener Sahin, Onur Erdogan, Can Sarica

المصدر: World Neurosurgery. 138:35-38

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::6764feaa56102c8bf3e23538841554a8Test
https://doi.org/10.1016/j.wneu.2020.02.118Test

2

Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus

المؤلفون: Edith Mbabazi Kabachelor, William E. Butler, James M. Johnston, Kristopher T. Kahle, Carol Nelson-Williams, James R. Broach, Kaya Bilguvar, August A Allocco, Laura R. Ment, Andrew T. Timberlake, Peña, Peter Ssenyonga, Shozeb Haider, Christopher Castaldi, Arnaud Marlier, Bulent Guclu, Xue Zen, Steven J. Schiff, Rebecca L. Walker, Benjamin C. Reeves, James R. Knight, William J. Sullivan, Michael L. DiLuna, Weilai Dong, Bermans J. Iskandar, Yasar Bayri, Gregory G. Heuer, Boyang Li, Michael L.J. Apuzzo, Yener Sahin, Charuta G. Furey, Shreyas Panchagnula, Daniel H. Geschwind, Hannah Smith, Richard P. Lifton, Duy Phan, Michael C. Sierant, Sheng Chih Jin, Eric M. Jackson, Edward R. Smith, Tyrone DeSpenza, Irina Tikhonova, Murat Gunel, Andres Moreno-De-Luca, Nenad Sestan, Boris Keren, June Goto, Seth L. Alper, Charles C. Duncan, Adam J. Kundishora, Shrikant Mane, Ellen J. Hoffman, Francesco T. Mangano, Helena, Ashley Dunbar, Jason K. Karimy, Benjamin C. Warf, David D. Limbrick, Qiongshi Lu, Christine Hehnly, Sierra B Conine, Li Ge

المصدر: Neurosurgery. 67

مصطلحات موضوعية: Proband, business.industry, Neurogenesis, Genomics, Prenatal care, Bioinformatics, Congenital hydrocephalus, Neuron differentiation, Medicine, Surgery, Neurology (clinical), business, Neural development, Exome

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::2c037174cfc0082a75a8d10c5f0695ebTest
https://doi.org/10.1093/neuros/nyaa447_572Test

3

Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus

المؤلفون: William J. Sullivan, Bermans J. Iskandar, Yasar Bayri, James R. Knight, James M. Johnston, Michael L.J. Apuzzo, Kristopher T. Kahle, Boyang Li, Andrew T. Timberlake, Sheng Chih Jin, Steven J. Schiff, Shreyas Panchagnula, Rebecca L. Walker, Shozeb Haider, Li Ge, Daniel H. Geschwind, Hannah Smith, Richard P. Lifton, Seth L. Alper, Carol Nelson-Williams, Boris Keren, Christine Hehnly, Arnaud Marlier, Bulent Guclu, Laura R. Ment, Ellen J. Hoffman, Francesco T. Mangano, Xue Zeng, Edith Mbabazi Kabachelor, Kaya Bilguvar, August A Allocco, Ashley Dunbar, James R. Broach, Benjamin C. Warf, William E. Butler, Helena Perez Pena, Sierra B Conine, David D. Limbrick, Qiongshi Lu, Edward R. Smith, Jason K. Karimy, Christopher Castaldi, Eric M. Jackson, Yener Sahin, Murat Gunel, Adam J. Kundishora, Charles C. Duncan, Michael L. DiLuna, Shrikant Mane, Michael C. Sierant, Gregory G. Heuer, June Goto, Charuta G. Furey, Andres Moreno-De-Luca, Peter Ssenyonga, Weilai Dong, Nenad Sestan, Phan Q. Duy, Benjamin C. Reeves, Tyrone DeSpenza, Irina Tikhonova

المساهمون: Jin, Sheng Chih, Dong, Weilai, Kundishora, Adam J., Panchagnula, Shreyas, Moreno-De-Luca, Andres, Furey, Charuta G., Allocco, August A., Walker, Rebecca L., Nelson-Williams, Carol, Smith, Hannah, Dunbar, Ashley, Conine, Sierra, Lu, Qiongshi, Zeng, Xue, Sierant, Michael C., Knight, James R., Sullivan, William, Duy, Phan Q., DeSpenza, Tyrone, Reeves, Benjamin C., Karimy, Jason K., Marlier, Arnaud, Castaldi, Christopher, Tikhonova, Irina R., Li, Boyang, Pena, Helena Perez, Broach, James R., Kabachelor, Edith M., Ssenyonga, Peter, Hehnly, Christine, Ge, Li, Keren, Boris, Timberlake, Andrew T., Goto, June, Mangano, Francesco T., Johnston, James M., Butler, William E., Warf, Benjamin C., Smith, Edward R., Schiff, Steven J., Limbrick, David D., Jr., Heuer, Gregory, Jackson, Eric M., Iskandar, Bermans J., Mane, Shrikant, Haider, Shozeb, Guclu, Bulent, Bayri, Yasar, Sahin, Yener, Duncan, Charles C., Apuzzo, Michael L. J., DiLuna, Michael L., Hoffman, Ellen J., Sestan, Nenad, Ment, Laura R., Alper, Seth L., Bilguvar, Kaya, Geschwind, Daniel H., Gunel, Murat, Lifton, Richard P., Kahle, Kristopher T.

المصدر: Nat Med

مصطلحات موضوعية: EXPRESSION, 0301 basic medicine, Male, PTEN, Cell type, Neurogenesis, Ubiquitin-Protein Ligases, CHILDREN, Disease, VENTRICULAR ZONE DISRUPTION, Bioinformatics, General Biochemistry, Genetics and Molecular Biology, Article, COWDEN-SYNDROME, Cerebral Ventricles, PATHWAY, Tripartite Motif Proteins, 03 medical and health sciences, 0302 clinical medicine, Cerebrospinal fluid, RARE, Neural Stem Cells, Pregnancy, Exome Sequencing, Medicine, Humans, Genetic Predisposition to Disease, Exome, AUTISM, Exome sequencing, Gliogenesis, SPECTRUM, Fetus, business.industry, Brain, General Medicine, medicine.disease, Neural stem cell, DE-NOVO MUTATION, 030104 developmental biology, 030220 oncology & carcinogenesis, Mutation, Female, business, Neuroglia, Ventriculomegaly, Transcription Factors, Hydrocephalus