المؤلفون: Parishmita Barman, MBBS, Gaurav Vedprakash Mishra, MBBS, MD, G Murugan, MBBS, MD, Piyoosh Priyadarshee, MBBS, Mayur Wanjari, MSc, Anshul Sood, MBBS

المصدر: Radiology Case Reports, Vol 20, Iss 4, Pp 2004-2008 (2025)

مصطلحات موضوعية: Brain malformation, Holoprosencephaly, Interhemispheric fissure, Lobar, Meningocele, Seizures, Medical physics. Medical radiology. Nuclear medicine, R895-920

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S1930043325000287; https://doaj.org/toc/1930-0433

URL الوصول: https://doaj.org/article/0f4a1ebe9def4632bff81a902396c468

المؤلفون: A. A. Lebedenko, A. A. Afonin, T. B. Kozyreva, K. I. Lazareva, L. I. Monat

المصدر: Медицинский вестник Юга России, Vol 15, Iss 2, Pp 101-111 (2024)

مصطلحات موضوعية: newborn, brain malformation, children, peroxisome diseases, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://www.medicalherald.ru/jour/article/view/1697; https://doaj.org/toc/2219-8075; https://doaj.org/toc/2618-7876

URL الوصول: https://doaj.org/article/482915b347ab4b6aa532a0ab56b6e422

المؤلفون: Ndu Ik, Chinawa JM, Chikani M, Ibekwe R, Aronu AE, Edelu BO, Asinobi I

المصدر: Nigerian Journal of Paediatrics, Vol 42, Iss 1, Pp 73-75 (2024)

مصطلحات موضوعية: dandy walker syndrome, congenital brain malformation, childhood blindness, hydrocephalus, Medicine

وصف الملف: electronic resource

Relation: https://www.njpaediatrics.com/index.php/njp/article/view/298; https://doaj.org/toc/0302-4660; https://doaj.org/toc/2814-2985

URL الوصول: https://doaj.org/article/75635361fb7b4439abe69ed92a3168a6

المؤلفون: Qian, Xuyu, DeGennaro, Ellen, Talukdar, Maya, Akula, Shyam, Lai, Abbe, Shao, Diane, Gonzalez, Dilenny, Marciano, Jack, Smith, Richard, Hylton, Norma, Yang, Edward, Bazan, J, Barrett, Lee, Yeh, Rebecca, Hill, R, Beck, Samantha, Otani, Aoi, Angad, Jolly, Mitani, Tadahiro, Posey, Jennifer, Pehlivan, Davut, Calame, Daniel, Aydin, Hatip, Yesilbas, Osman, Parks, Kendall, England, Eleina, Im, Kiho, Taranath, Ajay, Scott, Hamish, Barnett, Christopher, Arts, Peer, Sherr, Elliott, Lupski, James, Walsh, Christopher, Argilli, Emanuela

المصدر: Developmental Cell. 57(20)

مصطلحات موضوعية: apoptosis, cerebral cortex, congenital brain malformation, corpus callosum, development, genetics, kinesin, migration, organoid, Humans, Animals, Mice, Kinesins, Neurons, Focal Adhesion Protein-Tyrosine Kinases, Apoptosis, Brain

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/9rq571mk
https://escholarship.org/content/qt9rq571mk/qt9rq571mk.pdf

المؤلفون: Dmytro V. Shchehlov, Oleh Ye. Svyrydiuk, Mykola B. Vyval, Svitlana V. Chebanyuk, Igor V. Altman, Maryna Yu. Mamonova

المصدر: Український журнал серцево-судинної хірургії, Vol 31, Iss 3, Pp 127-133 (2023)

مصطلحات موضوعية: brain malformation, endovascular treatment, intracranial hemorrhage, outcome, modified rankin scale, eq-5d-3l questionnaire, Surgery, RD1-811

وصف الملف: electronic resource

Relation: http://cvs.org.ua/index.php/ujcvs/article/view/590; https://doaj.org/toc/2664-5963; https://doaj.org/toc/2664-5971

URL الوصول: https://doaj.org/article/f14920b6835a4952b53ba968accfe5c7

المؤلفون: Haizhu Chen, Ying Zheng, Hua Wu, Naiqing Cai, Guorong Xu, Yi Lin, Jin-Jing Li

المصدر: Frontiers in Neurology, Vol 15 (2024)

مصطلحات موضوعية: microcephaly, autosomal recessive primary microcephaly type 2, WDR62 mutation, epilepsy, consanguineous marriage, brain malformation, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fneur.2024.1341864/full; https://doaj.org/toc/1664-2295

URL الوصول: https://doaj.org/article/f63a3d526d974c7ca4072f172e4be996

المؤلفون: M Mieszkowska, K Michalska, M Mieszkowski, M Dowgierd, Y Zhalniarovich

المصدر: Veterinární Medicína, Vol 68, Iss 8, Pp 343-348 (2023)

مصطلحات موضوعية: intracranial cyst, congenital brain malformation, mri, Veterinary medicine, SF600-1100

وصف الملف: electronic resource

Relation: https://vetmed.agriculturejournals.cz/artkey/vet-202308-0003_a-quadrigeminal-arachnoid-cyst-as-a-cause-of-neurological-symptoms-in-an-11-month-old-brussels-griffon-8211.php; https://doaj.org/toc/0375-8427; https://doaj.org/toc/1805-9392

URL الوصول: https://doaj.org/article/41f9264b75f0443dbb6a5ca9a3b7bc84

المؤلفون: Jeanne, Médéric, Demory, Hélène, Moutal, Aubin, Vuillaume, Marie-Laure, Blesson, Sophie, Thépault, Rose-Anne, Marouillat, Sylviane, Halewa, Judith, Maas, Saskia M, Motazacker, M Mahdi, Mancini, Grazia MS, van Slegtenhorst, Marjon A, Andreou, Avgi, Cox, Helene, Vogt, Julie, Laufman, Jason, Kostandyan, Natella, Babikyan, Davit, Hancarova, Miroslava, Bendova, Sarka, Sedlacek, Zdenek, Aldinger, Kimberly A, Sherr, Elliott H, Argilli, Emanuela, England, Eleina M, Audebert-Bellanger, Séverine, Bonneau, Dominique, Colin, Estelle, Denommé-Pichon, Anne-Sophie, Gilbert-Dussardier, Brigitte, Isidor, Bertrand, Küry, Sébastien, Odent, Sylvie, Redon, Richard, Khanna, Rajesh, Dobyns, William B, Bézieau, Stéphane, Honnorat, Jérôme, Lohkamp, Bernhard, Toutain, Annick, Laumonnier, Frédéric

المصدر: American Journal of Human Genetics. 108(5)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Rare Diseases, Neurosciences, Brain Disorders, Pediatric, Intellectual and Developmental Disabilities (IDD), Mental Health, Aetiology, 2.1 Biological and endogenous factors, Mental health, Neurological, Adult, Agenesis of Corpus Callosum, Cerebellum, Child, Child, Preschool, Female, Humans, Hydrolases, Intellectual Disability, Male, Microtubule-Associated Proteins, Models, Molecular, Mutation, Missense, Neurodevelopmental Disorders, Tubulin, Young Adult, DPYSL5, brain malformation, corpus callosum agenesis, de novo missense variants, dendrite branching, neurodevelopmental disorder, primary neuronal cultures, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/9t75z0zj

المؤلفون: Nga Ying Eng, Duyu A. Nie

المصدر: Epilepsy & Behavior Reports, Vol 26, Iss , Pp 100664- (2024)

مصطلحات موضوعية: Infantile spasms, Encephalopathy, Cytomegalovirus, Brain malformation, Epilepsy, Neurology. Diseases of the nervous system, RC346-429, Neurophysiology and neuropsychology, QP351-495

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2589986424000212; https://doaj.org/toc/2589-9864

URL الوصول: https://doaj.org/article/c713b82e250b4d68802e22af5c878d33

المؤلفون: Yu, Yoshihiko, Creighton, Erica K, Buckley, Reuben M, Lyons, Leslie A, 99 Lives Consortium

المصدر: Genes. 11(6)

مصطلحات موضوعية: Lives Consortium, Animals, Cats, Mice, Hydrocephalus, Nervous System Malformations, Bone Morphogenetic Proteins, Pedigree, Genotype, Homozygote, Phenotype, Genome-Wide Association Study, Telencephalic Commissures, Whole Genome Sequencing, BMP12, Felis catus, brain malformation, feline, genetics, genome-wide association study, genomics, mendelian traits, neurodevelopment, whole genome sequencing, Genetics

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3d81p5jx

المؤلفون: Wei Shern Lee, Emma Macdonald‐Laurs, Sarah E M Stephenson, Colleen D'Arcy, Duncan MacGregor, Richard J Leventer, Wirginia Maixner, A Simon Harvey, Paul J Lockhart

المصدر: Epilepsia Open, Vol 8, Iss 1, Pp 205-210 (2023)

مصطلحات موضوعية: brain malformation, dysmorphic neuron, epilepsy, genetics, somatic mosaicism, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2470-9239

URL الوصول: https://doaj.org/article/43a28f90c6074072b7d54c233d653d34

المؤلفون: Johnson, Brett V, Kumar, Raman, Oishi, Sabrina, Alexander, Suzy, Kasherman, Maria, Vega, Michelle Sanchez, Ivancevic, Atma, Gardner, Alison, Domingo, Deepti, Corbett, Mark, Parnell, Euan, Yoon, Sehyoun, Oh, Tracey, Lines, Matthew, Lefroy, Henrietta, Kini, Usha, Van Allen, Margot, Grønborg, Sabine, Mercier, Sandra, Küry, Sébastien, Bézieau, Stéphane, Pasquier, Laurent, Raynaud, Martine, Afenjar, Alexandra, Billette de Villemeur, Thierry, Keren, Boris, Désir, Julie, Van Maldergem, Lionel, Marangoni, Martina, Dikow, Nicola, Koolen, David A, VanHasselt, Peter M, Weiss, Marjan, Zwijnenburg, Petra, Sa, Joaquim, Reis, Claudia Falcao, López-Otín, Carlos, Santiago-Fernández, Olaya, Fernández-Jaén, Alberto, Rauch, Anita, Steindl, Katharina, Joset, Pascal, Goldstein, Amy, Madan-Khetarpal, Suneeta, Infante, Elena, Zackai, Elaine, Mcdougall, Carey, Narayanan, Vinodh, Ramsey, Keri, Mercimek-Andrews, Saadet, Pena, Loren, Shashi, Vandana, Undiagnosed Diseases Network, Schoch, Kelly, Sullivan, Jennifer A, Pinto E Vairo, Filippo, Pichurin, Pavel N, Ewing, Sarah A, Barnett, Sarah S, Klee, Eric W, Perry, M Scott, Koenig, Mary Kay, Keegan, Catherine E, Schuette, Jane L, Asher, Stephanie, Perilla-Young, Yezmin, Smith, Laurie D, Rosenfeld, Jill A, Bhoj, Elizabeth, Kaplan, Paige, Li, Dong, Oegema, Renske, van Binsbergen, Ellen, van der Zwaag, Bert, Smeland, Marie Falkenberg, Cutcutache, Ioana, Page, Matthew, Armstrong, Martin, Lin, Angela E, Steeves, Marcie A, Hollander, Nicolette den, Hoffer, Mariëtte JV, Reijnders, Margot RF, Demirdas, Serwet, Koboldt, Daniel C, Bartholomew, Dennis, Mosher, Theresa Mihalic, Hickey, Scott E, Shieh, Christine, Sanchez-Lara, Pedro A, Graham, John M, Tezcan, Kamer, Schaefer, GB, Danylchuk, Noelle R, Asamoah, Alexander, Jackson, Kelly E, Yachelevich, Naomi, Au, Margaret, Pérez-Jurado, Luis A, Kleefstra, Tjitske

المصدر: Biological psychiatry. 87(2)

مصطلحات موضوعية: Undiagnosed Diseases Network, Animals, Humans, Mice, Ubiquitin Thiolesterase, Transforming Growth Factor beta, Developmental Disabilities, Signal Transduction, Phenotype, Female, Male, Haploinsufficiency, Intellectual Disability, Brain malformation, Deubiquitylating enzyme, Hippocampus, Neurodevelopmental disorder, TGFβ, USP9X, Congenital Structural Anomalies, Genetics, Neurosciences, Pediatric, Mental Health, Behavioral and Social Science, Brain Disorders, Clinical Research, 2.1 Biological and endogenous factors, Aetiology, Neurological, TGF beta, Biological Sciences, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/7rc8p7tf

المؤلفون: Yan-Ting Lu, Chung-Yao Hsu, Yo-Tsen Liu, Chung-Kin Chan, Yao-Chung Chuang, Chih-Hsiang Lin, Kai-Ping Chang, Chen-Jui Ho, Ching-Ching Ng, Kheng-Seang Lim, Meng-Han Tsai

المصدر: Biomedical Journal, Vol 45, Iss 3, Pp 542-548 (2022)

مصطلحات موضوعية: Periventricular heterotopia, MRI, Epilepsy, Brain malformation, FLNA, Medicine (General), R5-920, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2319417021000603; https://doaj.org/toc/2319-4170

URL الوصول: https://doaj.org/article/22ca7cdfa34d4817a703a5af7b78f1bf

المؤلفون: Kristin Barañano, Irina Burd

المصدر: Maternal Health, Neonatology and Perinatology, Vol 8, Iss 1, Pp 1-7 (2022)

مصطلحات موضوعية: Brain malformation, Agenesis corpus callosum, Ventriculomegaly, Dandy Walker malformation, Medicine

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2054-958X

URL الوصول: https://doaj.org/article/bd30d6dabf0e4eeba29a8782aee85986

المؤلفون: Fileva, Nevena, Severino, Mariasavina, Tortora, Domenico, Ramaglia, Antonia, Paladini, Dario, Rossi, Andrea

المساهمون: Fileva, Nevena, Severino, Mariasavina, Tortora, Domenico, Ramaglia, Antonia, Paladini, Dario, Rossi, Andrea

مصطلحات موضوعية: brain malformation, cortical malformation, fetal brain MRI, posterior fossa

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000933224600008; volume:51; issue:2; numberofpages:17; journal:JOURNAL OF CLINICAL ULTRASOUND; https://hdl.handle.net/11588/989615

الاتاحة: https://hdl.handle.net/11588/989615
https://doi.org/10.1002/jcu.23423
https://onlinelibrary.wiley.com/doi/10.1002/jcu.23423

المؤلفون: Raissa Rilo Christoff, Jefferson H. Quintanilha, Raiane Oliveira Ferreira, Jessica C. C. G. Ferreira, Daniel Menezes Guimarães, Bruna Valério-Gomes, Luiza M. Higa, Átila D. Rossi, Maria Bellio, Amilcar Tanuri, Roberto Lent, Patricia Pestana Garcez

المصدر: Viruses, Vol 15, Iss 12, p 2336 (2023)

مصطلحات موضوعية: axon growth, axon guidance, brain malformation, congenital Zika syndrome, corticogenesis, callosal dysgenesis, Microbiology, QR1-502

Relation: https://www.mdpi.com/1999-4915/15/12/2336; https://doaj.org/toc/1999-4915; https://doaj.org/article/c2ac876340f5467a9f79b9c180d43aa6

الاتاحة: https://doi.org/10.3390/v15122336
https://doaj.org/article/c2ac876340f5467a9f79b9c180d43aa6

المؤلفون: Gabriele Amorosino, Denis Peruzzo, Daniela Redaelli, Emanuele Olivetti, Filippo Arrigoni, Paolo Avesani

المصدر: NeuroImage, Vol 260, Iss , Pp 119486- (2022)

مصطلحات موضوعية: Brain tissue segmentation, Brain malformation, Machine learning, Supervised learning, Benchmark, Magnetic resonance imaging (MRI), Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S1053811922006024; https://doaj.org/toc/1095-9572

URL الوصول: https://doaj.org/article/93f7788e84244d3ba0636df1020fb8b8

المؤلفون: D. M. Guseva, T. V. Markova, L. A. Bessonova, S. S. Nikitin, E. L. Dadali, O. A. Shchagina

المصدر: Нервно-мышечные болезни, Vol 11, Iss 1, Pp 19-24 (2021)

مصطلحات موضوعية: brain malformation, lissencephaly, microcephaly, tubulin, tuba1a, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://nmb.abvpress.ru/jour/article/view/423; https://doaj.org/toc/2222-8721; https://doaj.org/toc/2413-0443

URL الوصول: https://doaj.org/article/4df255bf4c264de8b16af0b0f9557ea1

المؤلفون: Maryam Mohd Zulkifli, Siti Balqis Channmekun, Siti Suhaila Mohd Yusoff, Rosediani Muhamad, Ahmad Tarmizi Musa

المصدر: Malaysian Family Physician, Vol 15, Iss 3, Pp 90-94 (2020)

مصطلحات موضوعية: brain malformation, development delay, hemiparesis, schizencephaly, Medicine

وصف الملف: electronic resource

Relation: https://e-mfp.org/wp-content/uploads/v15n3-case-report-5.pdf; https://doaj.org/toc/1985-207X; https://doaj.org/toc/1985-2274

URL الوصول: https://doaj.org/article/7c303cb6e6ff4789bceac16875adaff6

المؤلفون: Masashi Ueda, Tohru Matsuki, Masahide Fukada, Shima Eda, Akie Toya, Akio Iio, Hidenori Tabata, Atsuo Nakayama

المصدر: Molecular Brain, Vol 13, Iss 1, Pp 1-9 (2020)

مصطلحات موضوعية: SON, Zhu-Tokita-Takenouchi-Kim syndrome, Brain malformation, Intellectual disability, Neuronal migration, Spinogenesis, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13041-020-00622-4; https://doaj.org/toc/1756-6606

URL الوصول: https://doaj.org/article/407a176e363f46fca3b22304b6db3edc