المؤلفون: Karina Lidia Gheorghita, A.V. Ciurea, R.E. Rizea

المصدر: Romanian Neurosurgery, Vol 37, Iss 3 (2023)

مصطلحات موضوعية: YWHAG, developmental and epileptic encephalopathy, neurocognitive disorder, autistic spectrum disorder, polymorphic seizures, Arnold-Chiari malformation type I, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: http://journals.lapub.co.uk/index.php/roneurosurgery/article/view/2571; https://doaj.org/toc/1220-8841; https://doaj.org/toc/2344-4959

URL الوصول: https://doaj.org/article/e5c8091630924228bb2304926fc3348e

المؤلفون: Gheorghita, Karina Lidia, Ciurea, A.V., Rizea, R.E.

المصدر: Romanian Neurosurgery; Vol. XXXVII, No. 3 (September 2023); 249-251 ; 2344-4959 ; 1220-8841

مصطلحات موضوعية: YWHAG, developmental and epileptic encephalopathy, neurocognitive disorder, autistic spectrum disorder, polymorphic seizures, Arnold-Chiari malformation type I, parietal dystrophy

وصف الملف: application/pdf

Relation: https://journals.lapub.co.uk/index.php/roneurosurgery/article/view/2571/1746; https://journals.lapub.co.uk/index.php/roneurosurgery/article/view/2571

الاتاحة: https://journals.lapub.co.uk/index.php/roneurosurgery/article/view/2571

المؤلفون: Florou C, Andreanos K, Georgakoulias N, Espinosa E, Papakonstantinou E, Georgalas I, Rotsos T

المصدر: International Medical Case Reports Journal, Vol Volume 13, Pp 657-661 (2020)

مصطلحات موضوعية: arnold chiari malformation type i, herniation of cerebellar tonsils, elevated optic disc, papilledema, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://www.dovepress.com/acute-visual-loss-secondary-to-arnold-chiari-type-i-malformation-compl-peer-reviewed-article-IMCRJ; https://doaj.org/toc/1179-142X

URL الوصول: https://doaj.org/article/ad207662bdc64a9cad536e652bd35241

المؤلفون: Gizewska-Kacprzak, K, Walaszek, I

المصدر: 14th Triennial Congress of the International Federation of Societies for Surgery of the Hand (IFSSH), 11th Triennial Congress of the International Federation of Societies for Hand Therapy (IFSHT), 11th Triennial Congress of the International Federation of Societies for Hand Therapy (IFSHT); 20190617-20190621; Berlin; DOCIFSSH19-1129 /20200206/

مصطلحات موضوعية: Dupuytren disease, Xiapex, Child, Arnold Chiari Malformation type I, ddc: 610

Relation: http://dx.doi.org/10.3205/19ifssh0431; http://nbn-resolving.de/urn:nbn:de:0183-19ifssh04311; http://www.egms.de/en/meetings/ifssh2019/19ifssh0431.shtml

الاتاحة: https://doi.org/10.3205/19ifssh0431
http://nbn-resolving.de/urn:nbn:de:0183-19ifssh04311
http://www.egms.de/en/meetings/ifssh2019/19ifssh0431.shtml

المؤلفون: Vijay Sardana, Rahi Kiran Bhattiprolu

المصدر: Clinical Dermatology Review, Vol 3, Iss 2, Pp 136-138 (2019)

مصطلحات موضوعية: arnold-chiari malformation type i, leprosy, syringomyelia, Dermatology, RL1-803

وصف الملف: electronic resource

Relation: http://www.cdriadvlkn.org/article.asp?issn=2542-551X;year=2019;volume=3;issue=2;spage=136;epage=138;aulast=Sardana; https://doaj.org/toc/2542-551X; https://doaj.org/toc/2542-5528

URL الوصول: https://doaj.org/article/3b782119efe149c983bcb6d593942888

المؤلفون: Castiglione, Alessandro, 1976, Guaran, V., Astolfi, L., Orioli, E., Zeri, G., Gemmati, D., Bovo, R., Montaldi, A., Alghisi, A., Martini, A.

المصدر: Cytogenetic and Genome Research. 141(4):243-259

مصطلحات موضوعية: Arnold-Chiari malformation type I, Choanal atresia, Chromosome 6p, Coagulation factor XIII, Congenital heart defects, Congenital ptosis, D-dimer, Hearing loss, Partial trisomy, Renal hypoplasia

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-98975
https://doi.org/10.1159/000353846

المؤلفون: Jun-Ichi Yokota, Yoko Yamaguchi, 山口 洋子, 横田 淳一

المصدر: Equilibrium Research. 2018, 77(3):143

المؤلفون: E A Yurkina, S V Lobzin

المصدر: Vestnik severo-zapadnogo gosudarstvennogo medicinskogo universiteta im. I.I. Mečnikova, Vol 6, Iss 4, Pp 86-93 (2014)

مصطلحات موضوعية: Platybasia, lcsh:R5-920, business.industry, basilar impression, craniovertebral abnormalities, platybasia, Scientific literature, medicine.disease, «tight» posterior cranial fossa, hydromyelia, Basilar Impression, Medicine, arnold-chiari malformation type i, business, lcsh:Medicine (General), Hydromyelia, Clinical psychology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f68084a9963234128bbdf27b1aae242d
https://journals.eco-vector.com/vszgmu/article/viewFile/8451/6820

المؤلفون: A. Montaldi, Alessandro Castiglione, A. Martini, A. Alghisi, Roberto Bovo, Valeria Guaran, Giulia Zeri, Donato Gemmati, Laura Astolfi, Elisa Orioli

مصطلحات موضوعية: Male, Proband, Pathology, Trisomy, Chromosomal translocation, Choanal atresia, Translocation, Genetic, Congenital, CHARGE syndrome, Arnold-Chiari malformation type I, Chromosome 6p, Coagulation factor XIII, Congenital heart defects, Congenital ptosis, D-dimer, Hearing loss, Partial trisomy, Renal hypoplasia, Abnormalities, Multiple, Arnold-Chiari Malformation, Base Sequence, Choanal Atresia, Chromosomes, Human, Pair 6, Cytogenetic Analysis, Female, Heart Defects, Congenital, Humans, Karyotype, Phenotype, Renal Insufficiency, Sequence Analysis, DNA, Molecular Biology, Genetics, Genetics (clinical), Heart Defects, Arnold-Chiari malformation, Sensorineural hearing loss, Pair 6, Abnormalities, Multiple, Sequence Analysis, Human, medicine.medical_specialty, Translocation, Biology, Chromosomes, Genetic, medicine, Multiplex ligation-dependent probe amplification, Coagulation FXIII, DNA, medicine.disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79719e9a15f2bbc5c4068be6a639414d
http://hdl.handle.net/11392/1839901