المؤلفون: H. N. Ozcan, B. Oguz, T. Salim, B. Talim, M. Haliloglu

المصدر: Journal of the Belgian Society of Radiology, Vol 98, Iss 2, Pp 79-81 (2015)

مصطلحات موضوعية: Liver neoplasms, in infants and children., Medical physics. Medical radiology. Nuclear medicine, R895-920

وصف الملف: electronic resource

العلاقة: https://www.jbsr.be/articles/770Test; https://doaj.org/toc/2514-8281Test

الوصول الحر: https://doaj.org/article/c1d1f3471bd74ca6918dacb48fee7b39Test

المؤلفون: R. K. J. Olsen, E. KoåˆaåTMã­kovã¡, T. A. Giancaspero, S. Mosegaard, V. Boczonadi, L. Matakoviä‡, A. Veauville Merllié, C. Terrile, T. Schwarzmayr, T. B. Haack, M. Auranen, P. Leone, M. Galluccio, A. Imbard, P. Gutierrez Rios, J. Palmfeldt, E. Graf, C. Vianey Saban, M. Oppenheim, M. Schiff, S. Pichard, O. Rigal, A. Pyle, P. F. Chinnery, V. Konstantopoulou, D. Mã¶slinger, R. G. Feichtinger, B. Talim, H. Topaloglu, T. Coskun, S. Gucer, A. Botta, E. Pegoraro, A. Malena, L. Vergani, D. Mazzã, M. Zollino, D. Ghezzi, C. Acquaviva, T. Tyni, A. Boneh, T. Meitinger, T. M. Strom, N. Gregersen, J. A. Mayr, R. Horvath, M. Barile, H. Prokisch

المساهمون: R.K.J. Olsen, E. KoåˆaåTMã­kovã¡, T.A. Giancaspero, S. Mosegaard, V. Boczonadi, L. Matakoviä‡, A. Veauville Merllié, C. Terrile, T. Schwarzmayr, T.B. Haack, M. Auranen, P. Leone, M. Galluccio, A. Imbard, P. Gutierrez Rio, J. Palmfeldt, E. Graf, C. Vianey Saban, M. Oppenheim, M. Schiff, S. Pichard, O. Rigal, A. Pyle, P.F. Chinnery, V. Konstantopoulou, D. Mã¶slinger, R.G. Feichtinger, B. Talim, H. Topaloglu, T. Coskun, S. Gucer, A. Botta, E. Pegoraro, A. Malena, L. Vergani, D. Mazzã, M. Zollino, D. Ghezzi, C. Acquaviva, T. Tyni, A. Boneh, T. Meitinger, T.M. Strom, N. Gregersen, J.A. Mayr, R. Horvath, M. Barile, H. Prokisch

مصطلحات موضوعية: adult, blotting, western, case-control studie, cells, cultured, electron transport, female, fibroblast, flavin-adenine dinucleotide, frameshift mutation, gene expression profiling, human, infant, newborn, liver, male, mitochondrial disease, multiple acyl coenzyme a dehydrogenase deficiency, muscle, skeletal, mutagenesis, site-directed, nucleotidyltransferase, protein binding, rna, messenger, real-time polymerase chain reaction, reverse transcriptase polymerase chain reaction, riboflavin

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27259049; info:eu-repo/semantics/altIdentifier/wos/WOS:000377286000008; volume:98; issue:6; firstpage:1130; lastpage:1145; numberofpages:16; journal:AMERICAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/2434/523684Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84971568098

الإتاحة: https://doi.org/10.1016/j.ajhg.2016.04.006Test
http://hdl.handle.net/2434/523684Test

المؤلفون: H. Özyürek, A. Aksoy, Ö. Köken, B. Talim

المصدر: Neuromuscular Disorders. 27:S111

مصطلحات موضوعية: Pathology, medicine.medical_specialty, Neurology, business.industry, Pediatrics, Perinatology and Child Health, medicine, Congenital muscular dystrophy, Neurology (clinical), Muscle disorder, medicine.disease, business, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::fae5a3c83c59e735f9f2efc172fc3228Test
https://doi.org/10.1016/j.nmd.2017.06.073Test

المؤلفون: E. Demir, K. Gucuyener, A. Akturk, B. Talim, O. Konus, S. Ghezzi, R. Del Bo, G.P. Comi

المساهمون: E. Demir, K. Gucuyener, A. Akturk, B. Talim, O. Konu, R. Del Bo, S. Ghezzi, G.P. Comi

مصطلحات موضوعية: MEB, Mild phenotype, Severe eye abnormalities, Settore MED/26 - Neurologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/19679478; info:eu-repo/semantics/altIdentifier/wos/WOS:000271366300005; volume:19; issue:10; firstpage:692; lastpage:695; journal:NEUROMUSCULAR DISORDERS; http://hdl.handle.net/2434/72164Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-70349388710

الإتاحة: https://doi.org/10.1016/j.nmd.2009.07.006Test
http://hdl.handle.net/2434/72164Test

المؤلفون: B, Balci, E, Wilichowski, G, Haliloğlu, B, Talim, S, Aurino, E, Kremer, F, Ebinger, N, Senbil, B, Anlar, G, Kale, V, Nigro, H, Topaloğlu, C, Bonnemann, P, Dinçer

المصدر: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology. 23(3)

مصطلحات موضوعية: Adult, Male, Adolescent, Turkey, Genetic Linkage, Exons, Severity of Illness Index, Cohort Studies, Phenotype, Muscular Dystrophies, Limb-Girdle, Sarcoglycans, Mutation, Humans, Female, Child

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::e34328423a2dc9a8dbb25c34155dd5e9Test
https://pubmed.ncbi.nlm.nih.gov/15938573Test

المؤلفون: G, Haliloglu, C, Gross, N, Senbil, B, Talim, U, Hehr, G, Uyanik, J, Winkler, H, Topaloglu

المصدر: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology. 23(3)

مصطلحات موضوعية: Male, Genetic Heterogeneity, Adolescent, Child, Preschool, Brain, Humans, Stereotypic Movement Disorder, Female, Eye Abnormalities, Autistic Disorder, N-Acetylglucosaminyltransferases, Severity of Illness Index, Muscular Dystrophies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::cdacddc518157b6c983dc5233912d23bTest
https://pubmed.ncbi.nlm.nih.gov/15938569Test

المؤلفون: B. GIUSTI, L. LUCARINI, V. PIETRONI, S. LUCIOLI, B. BANDINELLI, P. SABATELLI, S. SQUARZONI, S. PETRINI, C. GARTIOUX, B. TALIM, F. ROELENS, L. MERLINI, H. TOPALOGLU, E. BERTINI, P. GUICHENEY, G. PEPE

المصدر: Annals of neurology 58 (2005): 400–410.
info:cnr-pdr/source/autori:B. GIUSTI, L. LUCARINI, V. PIETRONI, S. LUCIOLI, B. BANDINELLI, P. SABATELLI, S. SQUARZONI, S. PETRINI, C. GARTIOUX, B. TALIM, F. ROELENS, L. MERLINI, H. TOPALOGLU, E. BERTINI, P. GUICHENEY, G. PEPE,/titolo:Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy,/doi:/rivista:Annals of neurology/anno:2005/pagina_da:400/pagina_a:410/intervallo_pagine:400–410/volume:58

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=cnr_________::5810bc1c86d184507a3cf447d451cf17Test
http://www.cnr.it/prodotto/i/5261Test

المؤلفون: P, Oğuzkurt, B, Talim, F C, Tanyel, M, Cağlar, M E, Senocak, N, Büyükpamukçu

المصدر: The Turkish journal of pediatrics. 43(4)

مصطلحات موضوعية: Male, Chi-Square Distribution, Adolescent, Helicobacter pylori, Infant, Newborn, Infant, Choristoma, Helicobacter Infections, Diagnosis, Differential, Meckel Diverticulum, Gastric Mucosa, Child, Preschool, Gastritis, Humans, Female, Child, Retrospective Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::9d8918362b341197dbd453b5e647e275Test
https://pubmed.ncbi.nlm.nih.gov/11765161Test

المؤلفون: I. Oncel, B. Talim, Benan Bayrakci, Selman Kesici, S. Ekinci, G. Kale

المصدر: Pediatric Critical Care Medicine. 15:7

مصطلحات موضوعية: Transplantation, medicine.medical_specialty, Hyperbaric oxygen, business.industry, Anesthesia, Pediatrics, Perinatology and Child Health, medicine, Critical Care and Intensive Care Medicine, business, Ex vivo, Surgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::e7accc3802a1f817570788897d5b2eaeTest
https://doi.org/10.1097/01.pcc.0000448745.01893.b0Test

المؤلفون: A, Oto, U, Aydingöz, N, Başgün, B, Talim, E, Karaağaoğlu, H, Topaloğlu

المصدر: The Turkish journal of pediatrics. 43(1)

مصطلحات موضوعية: Male, Infant, Magnetic Resonance Imaging, Muscular Dystrophies, Statistics, Nonparametric, Pelvis, Muscular Atrophy, Logistic Models, Thigh, Child, Preschool, Humans, Female, Child, Muscle, Skeletal, Retrospective Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::5f2daf392d3e0d34d2067707d69d12a2Test
https://pubmed.ncbi.nlm.nih.gov/11297158Test