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1دورية أكاديمية
المؤلفون: İlknur EROL, Özge SÜRMELİ ONAY, Zerrin YILMAZ, Özge ÖZER, Füsun ALEHAN, Feride ŞAHİN
المصدر: Cukurova Medical Journal, Vol 40, Iss 1, Pp 169-173 (2015)
مصطلحات موضوعية: 22q13.3 deletion syndrome, aphasia, epilepsy, mental retardation, 22q13.3 delesyon sendromu, afazi, epilepsi, mental retardasyon, Medicine (General), R5-920
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Barış Malbora, Zekai Avcı, Fulden Dönmez, Bülent Alioğlu, Esra Baskın, Füsun Alehan, Namık Özbek
المصدر: Turkish Journal of Hematology, Vol 27, Iss 3, Pp 168-176 (2010)
مصطلحات موضوعية: acute leukemia, aplastic anemia, posterior reversible leukoencephalopathy syndrome, tumor lysis syndrome, Diseases of the blood and blood-forming organs, RC633-647.5
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Barış Malbora, Zekai Avcı, Alev Hasanoğlu, Füsun Alehan, Namık Özbek
المصدر: Turkish Journal of Hematology, Vol 27, Iss 3, Pp 216-218 (2010)
مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5
وصف الملف: electronic resource
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المؤلفون: Luc Régal, Katie Clarkson, Katherine Lachlan, Kati J. Buckingham, Charles J. Waechter, F. Sessions Cole, Kimiyo Raymond, Rita Barone, Daisy Rymen, Derek Wong, Arve Vøllo, Gert Matthijs, Jay Shendure, Alina T. Midro, Erik A. Eklund, Hudson H. Freeze, Rudy Van Coster, Gregory M. Cooper, Jeffrey S. Rush, Sergey A. Shiryaev, Luísa Diogo, Philip James, Andrew J. Kornberg, Laurie A. Demmer, Jose E. Abdenur, Valerie Race, Maria Kibaek, Shawn O'Connor, Lynne A. Wolfe, Amarilis Sanchez-Valle, Agata Fiumara, Miao He, Raymond Y. Wang, Alex J. Fay, Martin Kircher, Rebecca D. Ganetzky, William A. Gahl, Erika Souche, Füsun Alehan, Amy Yang, Michael J. Bamshad, Himanshu Goel, S. Lane Rutledge, Jane E. Brumbaugh, Susan Sparks, Daniel Katz, Can Ficicioglu, Bobby G. Ng, Jaak Jaeken, Heidi Peters, Christina Lam, Gerard T. Berry, Liesbeth Keldermans, Eric Vilain, Tim Wood, Lyndsay A. Harshman, Deborah A. Nickerson, Pamela Trapane, Joy Yaplito-Lee
المصدر: Human Mutation. 37:653-660
مصطلحات موضوعية: Genetics, Mannosyltransferase, Mutation, Glycosylation, Mannose, Biology, medicine.disease_cause, Phenotype, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, N-linked glycosylation, chemistry, 030225 pediatrics, medicine, Biomarker (medicine), Lipid glycosylation, 030217 neurology & neurosurgery, Genetics (clinical)
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المؤلفون: Taner Sezer, Füsun Alehan, Oya Balci, Nilufer Bayraktar, Figen Özçay
المصدر: Journal of Child Neurology. 31:285-288
مصطلحات موضوعية: Male, Pediatrics, medicine.medical_specialty, Adolescent, Screening test, Duodenum, Tissue transglutaminase, Duodenal biopsy, Prevalence, Enzyme-Linked Immunosorbent Assay, Disease, 03 medical and health sciences, 0302 clinical medicine, Intellectual Disability, 030225 pediatrics, Healthy control, Intellectual disability, Humans, Medicine, Child, biology, business.industry, medicine.disease, Immunoglobulin A, Celiac Disease, Pediatrics, Perinatology and Child Health, Etiology, biology.protein, Physical therapy, Female, Neurology (clinical), business, Biomarkers, Blood Chemical Analysis, 030217 neurology & neurosurgery
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2beb80a098cddda8ca645ed62674a92d
https://doi.org/10.1177/0883073815589759 -
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المؤلفون: Füsun Alehan, Hadassah Goldberg-Stern, Taner Sezer, Miki Har-Gil, Michael Farkash, Nathan Watemberg
المصدر: Pediatric Neurology. 52:410-413
مصطلحات موضوعية: Male, Time Factors, Adolescent, Electroencephalography, Epilepsy, Developmental Neuroscience, Seizures, Hyperventilation, medicine, Humans, Child, Prospective cohort study, medicine.diagnostic_test, Brain, medicine.disease, Absence seizure, Neurology, Child, Preschool, Anesthesia, Pediatrics, Perinatology and Child Health, Female, Neurology (clinical), medicine.symptom, Psychology
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7
المؤلفون: Yasemin Özkale, Füsun Alehan, Özlem Alkan, Ilknur Erol
المصدر: Pediatric Neurology
مصطلحات موضوعية: Male, medicine.medical_specialty, Pediatrics, Oseltamivir, Turkey, Adolescent, Disease, multiple sclerosis, Single Center, Methylprednisolone, Article, Serology, chemistry.chemical_compound, children, Developmental Neuroscience, Clarithromycin, medicine, Humans, acute disseminated encephalomyelitis, adolescents, Child, Infusions, Intravenous, Retrospective Studies, business.industry, Multiple sclerosis, Encephalomyelitis, Acute Disseminated, Immunoglobulins, Intravenous, Infant, Alzheimer's disease, medicine.disease, Surgery, Neurology, chemistry, Child, Preschool, Pediatrics, Perinatology and Child Health, Acute disseminated encephalomyelitis, Female, Neurology (clinical), business, Follow-Up Studies, medicine.drug
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8
المؤلفون: Taner Sezer, Füsun Alehan, Hasan Kandemir
المصدر: International Journal of Neuroscience. 123:553-556
مصطلحات موضوعية: Male, Topiramate, Research design, Adolescent, Headache Disorders, Amitriptyline, Fructose, Group B, law.invention, Daily headache, Double-Blind Method, Randomized controlled trial, law, medicine, Humans, Child, Adverse effect, business.industry, General Neuroscience, General Medicine, Analgesics, Non-Narcotic, Anesthesia, Anticonvulsants, Female, Headaches, medicine.symptom, business, medicine.drug
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المؤلفون: Hannu Kalimo, Angela Schulz, Maria Kousi, Liisa Myllykangas, Anna-Elina Lehesjoki, Erik Riesch, Aarno Palotie, Füsun Alehan, Stella Calafato, Verneri Anttila, Outi Kopra, Johannes R Lemke, Eveliina Jakkula, Michael Alber, Meral Topçu, Sarenur Gökben
المساهمون: Çocuk Sağlığı ve Hastalıkları
المصدر: Journal of Medical Genetics. 49:391-399
مصطلحات موضوعية: Potassium Channels, Ataxia, Turkey, KCTD7, Blotting, Western, Intracellular Space, Single-nucleotide polymorphism, Progressive myoclonus epilepsy, Biology, Polymorphism, Single Nucleotide, Article, Mice, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Animals, Humans, Missense mutation, Cells, Cultured, Genetics (clinical), 030304 developmental biology, Brain Chemistry, Genetics & Heredity, 0303 health sciences, Genetic heterogeneity, Homozygote, Chromosome Mapping, Sequence Analysis, DNA, Myoclonic Epilepsies, Progressive, medicine.disease, Disease gene identification, Pedigree, 3. Good health, Phenotype, Microscopy, Fluorescence, Mutation, medicine.symptom, Myoclonus, 030217 neurology & neurosurgery
وصف الملف: text/plain
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المؤلفون: Umut Selda Bayrakci, Virginia Vega-Warner, Füsun Alehan, Fatih Ozaltin, Handan Ozdemir, Ayse Oner, Esra Baskin, Friedhelm Hildebrandt, Rita Horvath
المساهمون: Çocuk Sağlığı ve Hastalıkları
المصدر: Pediatric Nephrology. 26:1157-1161
مصطلحات موضوعية: Male, Nephrology, medicine.medical_specialty, Pathology, Nephrotic Syndrome, Biopsy, DNA Mutational Analysis, Cytochrome-c Oxidase Deficiency, medicine.disease_cause, Pediatrics, Article, Electron Transport Complex IV, Phosphoinositide Phospholipase C, Internal medicine, medicine, Humans, Cytochrome c oxidase, Genetic Predisposition to Disease, Mutation, Alkyl and Aryl Transferases, Sclerosis, PLCE1, biology, medicine.diagnostic_test, business.industry, Respiratory chain complex, Infant, Membrane Proteins, Urology & Nephrology, medicine.disease, Phenotype, Pediatrics, Perinatology and Child Health, biology.protein, Sensorineural hearing loss, business, Nephrotic syndrome
وصف الملف: text/plain