المؤلفون: Maria do Sameiro Barroso

المصدر: Antropologia Portuguesa, Iss 41 (2024)

مصطلحات موضوعية: Icono-diagnosis, palaeopathology, craniofacial dysostosis, Crouzon syndrome, Graeco-Roman medicine, Bracara Augusta, Anthropology, GN1-890, Ethnology. Social and cultural anthropology, GN301-674

وصف الملف: electronic resource

Relation: https://impactum-journals.uc.pt/antropologiaportuguesa/article/view/14899; https://doaj.org/toc/0870-0990; https://doaj.org/toc/2182-7982

URL الوصول: https://doaj.org/article/55dc026bc8514bdfb2f8c00037cd05c0

المؤلفون: Federica Tiberio, Martina Salvati, Luca Polito, Giada Tisci, Alessia Vita, Ornella Parolini, Luca Massimi, Lorena Di Pietro, Pierpaolo Ceci, Gianpiero Tamburrini, Alessandro Arcovito, Elisabetta Falvo, Wanda Lattanzi

المصدر: Molecular Therapy: Nucleic Acids, Vol 36, Iss 1, Pp 102427- (2025)

مصطلحات موضوعية: MT: Oligonucleotides: Therapies and Applications, craniosynostosis, Crouzon syndrome, small interfering RNA, ferritin nanoparticles, gene silencing, Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2162253124003147; https://doaj.org/toc/2162-2531

URL الوصول: https://doaj.org/article/5ce506076369457291afcadd01f66806

المؤلفون: G. Popescu, Fl. Chindris, C.M. Andrasi, M.C. Zaharia, R.M. Gorgan

المصدر: Romanian Neurosurgery, Vol 38, Iss Special Issue (2024)

مصطلحات موضوعية: Crouzon syndrome, olfactory groove meningioma, intracranial meningioma, aneurysmal complexes, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: http://journals.lapub.co.uk/index.php/roneurosurgery/article/view/2845; https://doaj.org/toc/1220-8841; https://doaj.org/toc/2344-4959

URL الوصول: https://doaj.org/article/5d93b646797640d0aa570f19770e0f04

المؤلفون: Magniez, Sarah Safia Lila

المساهمون: Silva, Cátia Carvalho, Repositório Institucional da Universidade Fernando Pessoa

مصطلحات موضوعية: Cranioestenoses sindrómicas, Síndrome de Crouzon, Síndrome de Pfeiffer, Síndrome de Apert, Manifestações orais, Atendimento odontopediátrico, Syndromic craniostenoses, Crouzon syndrome, Pfeiffer syndrome, Apert syndrome, Oral manifestations, Pediatric dental care, Pediatric dentistry, Domínio/Área Científica::Ciências Médicas::Medicina Clínica

وصف الملف: application/pdf

الاتاحة: http://hdl.handle.net/10284/12695

المؤلفون: Zahra Sadat Modarresi, Narges Hajiani, Zeinab Bakhtiari, Farnoush Mohammadi

المصدر: Clinical Case Reports, Vol 12, Iss 7, Pp n/a-n/a (2024)

مصطلحات موضوعية: bleeding, case report, cranial sutures, craniofacial, Crouzon syndrome, von Willebrand disease, Medicine, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2050-0904

URL الوصول: https://doaj.org/article/61a300362a114a0ba9cd07892660f805

المؤلفون: Neeharika P Shah, Omkar N Gadre

المصدر: TNOA Journal of Ophthalmic Science and Research, Vol 62, Iss 1, Pp 117-120 (2024)

مصطلحات موضوعية: craniosynostosis, crouzon syndrome, ocular features, Ophthalmology, RE1-994

وصف الملف: electronic resource

Relation: http://www.tnoajosr.com/article.asp?issn=2589-4528;year=2024;volume=62;issue=1;spage=117;epage=120;aulast=Shah; https://doaj.org/toc/2589-4528; https://doaj.org/toc/2589-4536

URL الوصول: https://doaj.org/article/f20bb0d8e4234636aa87645e8658b89a

المؤلفون: Hossam Hassan Fawzy, Hesham Abo Rahma, Moaz Elsheikh, Mohamed Abdalla Elnahas, Khaled Adel Eid, Yasser Elsheikh

المصدر: Oral and Maxillofacial Surgery Cases, Vol 10, Iss 1, Pp 100345- (2024)

مصطلحات موضوعية: Computer-assisted surgery, 3D printing, Craniofacial dysostosis, Craniosynostosis, Hypertelorism, Crouzon disease, Surgery, RD1-811

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2214541924000014; https://doaj.org/toc/2214-5419

URL الوصول: https://doaj.org/article/5567d174f51a4700acd7e90c7c26f5aa

المؤلفون: Nobuhiro Ando, Nobuyuki Mitsukawa, Minoru Hayashi, Koichi Higaki, Yoshitaka Kubota

المصدر: Journal of Plastic and Reconstructive Surgery, Vol 2, Iss 3, Pp 102-106 (2023)

مصطلحات موضوعية: human tail, crouzon syndrome, fgfr2, Surgery, RD1-811

وصف الملف: electronic resource

Relation: https://www.jstage.jst.go.jp/article/jprs/2/3/2_2022-0031/_pdf/-char/en; https://doaj.org/toc/2436-259X

URL الوصول: https://doaj.org/article/f5707604d0f648328795dc47060d47a4

المؤلفون: García Arce, Kenia Lisis, Murguia Moré, Merling

المصدر: Paideia Revista de Educación; No. 72 (2023); 36-48 ; Paideia Revista de Educación ; Núm. 72 (2023); 36-48 ; 2452-5154 ; 0716-4815

مصطلحات موضوعية: Logopedia, Fonoaudiología, Síndrome de Crouzon, Estrategias de comunicación, Escolar

وصف الملف: application/pdf

Relation: https://revistas.udec.cl/index.php/paideia/article/view/18401/16482; https://revistas.udec.cl/index.php/paideia/article/view/18401

الاتاحة: https://revistas.udec.cl/index.php/paideia/article/view/18401
https://doi.org/10.29393/PA72-2AIGM30002

المؤلفون: Leite Pereira, João Pedro, Ghizoni, Enrico, Raposo-Amaral, Cássio Eduardo

المصدر: Archives of Pediatric Neurosurgery; Vol. 6 No. 3 (2024): Archives of Pediatric Neurosurgery; e2642024 ; 2675-3626 ; 10.46900/v6i3

مصطلحات موضوعية: craniosynostosis, PVDO, Posterior distraction, Apert syndrome, Crouzon syndrome

وصف الملف: application/pdf

Relation: https://www.archpedneurosurg.com.br/sbnped2019/article/view/264/234; https://www.archpedneurosurg.com.br/sbnped2019/article/view/264

الاتاحة: https://www.archpedneurosurg.com.br/sbnped2019/article/view/264
https://doi.org/10.46900/apn.v6i3.264

المؤلفون: Ajami, Sara, Van den Dam, Zoe, Hut, Julia, Savery, Dawn, Chin, Milton, Koudstaal, Maarten, Steacy, Miranda, Carriero, Alessandra, Pitsillides, Andrew, Chang, Y-M, Rau, Christoph, Marathe, Shashidhara, Dunaway, David, Jeelani, Noor Ul Owase, Schievano, Silvia, Pauws, Erwin, Borghi, Alessandro

المصدر: Journal of Anatomy (2024) (In press).

مصطلحات موضوعية: bone, craniofacial, craniosynostosis, Crouzon, FGFR2

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10196094/1/Pauws_Journal%20of%20Anatomy%20-%202024%20-%20Ajami.pdf; https://discovery.ucl.ac.uk/id/eprint/10196094/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10196094/1/Pauws_Journal%20of%20Anatomy%20-%202024%20-%20Ajami.pdf
https://discovery.ucl.ac.uk/id/eprint/10196094/

المؤلفون: Bilal Bengana

مصطلحات موضوعية: Rheumatology and arthritis, Syndorme de Crouzon, orthodontie, anomalies cranio-faciales

Relation: https://figshare.com/articles/journal_contribution/Syndrome_de_Crouzon_d_couverte_tardive_en_orthodontie/25112684

الاتاحة: https://doi.org/10.6084/m9.figshare.25112684.v1
https://figshare.com/articles/journal_contribution/Syndrome_de_Crouzon_d_couverte_tardive_en_orthodontie/25112684

المؤلفون: M. A. Sokolova, E. A. Sarkisyan, P. V. Shumilov, L. D. Vorona, L. A. Levchenko, Yu. L. Ishutina, E. I. Shabelnikova, A. I. Krapivkin, М. А. Соколова, Е. А. Саркисян, П. В. Шумилов, Л. Д. Ворона, Л. А. Левченко, Ю. Л. Ишутина, Е. И. Шабельникова, А. И. Крапивкин

المصدر: Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics); Том 69, № 1 (2024); 78-85 ; Российский вестник перинатологии и педиатрии; Том 69, № 1 (2024); 78-85 ; 2500-2228 ; 1027-4065

مصطلحات موضوعية: ген FGFR3, Crouzon syndrome, craniosynostosis, exophthalmos, hypertelorism, maxillary micrognathia, FGFR2 gene, FGFR3 gene, синдром Крузона, краниосиностоз, экзофтальм, гипертелоризм, микрогнатия верхней челюсти, ген FGFR2

وصف الملف: application/pdf

Relation: https://www.ped-perinatology.ru/jour/article/view/1942/1462; Sawh-Martinez R., Steinbacher D.M. Syndromic Craniosynostosis. Clin Plast Surg 2019; 46(2): 141–155. DOI:10.1016/j.cps.2018.11.009; Conrady C.D., Patel B.C. Crouzon Syndrome. StatPearls Publishing; 2023 Aug; PMID: 30085540. https://www.ncbi.nlm.nih.gov/books/NBK518998 / Ссылка активна на 12. 12. 2023.; Кулаков А.А. Челюстно-лицевая хирургия. Под ред. А.А. Кулакова. Москва: ГЭОТАР-Медиа, 2019; 692 с.; Cunningham M.L., Seto M.L., Ratisoontorn C., Heike C.L., Hing A.V. Syndromic craniosynostosis: from history to hydrogen bonds. Orthod Craniofac Res 2007; 10(2): 67–81. DOI:10.1111/j.1601–6343.2007.00389.x; Pal U.S., Gupta C., Chellappa A.A. Crouzon syndrome with primary optic nerve atrophy and normal brain functions : A case report. J Oral Biol Craniofac Res 2012; 2(2): 116–118. DOI:10.1016/j.jobcr.2012.03.011; Reardon W., Winter R.M., Rutland P., Pulleyn L.J., Jones B.M., Malcolm S. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome. Nat Genet 1994; 8(1): 98–103.; Di Rocco F., Collet C., Legeai-Mallet L., Arnaud E., Le Merrer M., Hadj-Rabia S., Renier D. Crouzon syndrome with acanthosis nigricans: a case-based update. Childs Nerv Syst 2011; 27(3): 349–354. DOI:10.1007/s00381–010–1347-z; Mathijssen I.M. Guideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on Craniosynostosis. J Craniofac Surg 2015; 26(6): 1735–1807. URL: https://www.researchgate.net/publication/281682735_Guideline_for_Care_of_Patients_With_the_Diagnoses_of_Craniosynostosis_Working_Group_on_Craniosynostosis; Kim H.J., Roh H.G., Lee I.W. Craniosynostosis: Updates in Radiologic Diagnosis. J Korean Neurosurg Soc 2016; 59(3): 219–226. DOI:10.3340/jkns.2016.59.3.219; Ciurea AV, Toader C. Genetics of craniosynostosis : review of the literature. J Med Life 2009; 2(1): 5–17.; Vargervik K., Rubin M.S., Grayson B.H., Figueroa A.A., Kreiborg S., Shirley J.C. et al. Parameters of care for craniosynostosis: dental and orthodontic perspectives. Am J Orthod Dentofacial Orthop 2012; 141(4 Suppl): S68–73. DOI:10.1016/j.ajodo.2011.12.013; Raybaud C., Di Rocco C. Brain malformation in syndromic craniosynostoses, a primary disorder of white matter : a review. Childs Nerv Syst 2007; 23(12): 1379–1388. DOI:10.1007/s00381–007–0474–7; Conrady C.D., Patel B.C., Sharma S. Apert Syndrome. Stat-Pearls Publishing; 2023 Jan; PMID: 30085535. https://pubmed.ncbi.nlm.nih.gov/30085535 / Ссылка активна на 12. 12. 2023.; Wilkie A.O., Slaney S.F., Oldridge M., Poole M.D., Ashworth G.J., Hockley A.D. et al. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nat Genet 1995; 9(2): 165–172.; Fearon J.A. Treatment of the hands and feet in Apert syndrome: an evolution in management. Plast Reconstr Surg 2003; 112(1): 1–12. URL: https://www.researchgate.net/publication/10685177_Treatment_of_the_Hands_and_Feet_in_Apert_Syndrome_An_Evolution_in_Management; Betances E.M., Mendez M.D., Das J. Craniosynostosis. Stat-Pearls Publishing 2023; PMID: 31335086. https://pubmed.ncbi.nlm.nih.gov/31335086 / Ссылка активна на 12.12.2023.; Kalathia M.B., Parikh Y.N., Dhami M.D., Hapani P.T. Pfeiffer syndrome. J Pediatr Neurosci 2014; 9(1): 85–86. URL: https://www.researchgate.net/publication/262816749_Pfeiffer_syndrome; Клинические рекомендации ассоциации генетиков и неврологов 2017 «Диагностика и лечение синдрома Пфайффера». https://med-gen.ru/docs/pfayfer.pdf / Ссылка активна на 12. 12. 2023.; Taylor J.A., Bartlett S.P. What’s New in Syndromic Craniosynostosis Surgery? Plast Reconstr Surg 2017; 140(1): 82e–93e. URL: https://www.researchgate.net/publication/318163206_What's_New_in_Syndromic_Craniosynostosis_Surgery; Azoury S.C., Reddy S., Shukla V., Deng C.X. Fibroblast Growth Factor Receptor 2 (FGFR2) Mutation Related Syndromic Craniosynostosis. Int J Biol Sci 2017; 13(12): 1479–1488. DOI:10.7150/ijbs.22373; Graul-Neumann L.M., Klopocki E., Adolphs N., Mensah M.A., Kress W. Mutation c.943G>T (p.Ala315Ser) in FGFR2 Causing a Mild Phenotype of Crouzon Craniofacial Dysostosis in a Three-Generation Family. Mol Syndromol 2017; 8(2): 93–97. DOI:10.1159/000455028; Kutkowska-Kaźmierczak A., Gos M., Obersztyn E. Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling. J Appl Genet 2018; 59(2) :133–147. DOI:10.1007/s13353–017–0423–4; Snyder-Warwick A.K., Perlyn C.A., Pan J., Yu K., Zhang L., Ornitz D.M. Analysis of a gain-of-function FGFR2 Crouzon mutation provides evidence of loss of function activity in the etiology of cleft palate. Proc Natl Acad Sci USA 2010; 107(6): 2515–20. DOI:10.1073/pnas.0913985107; Carter E.P., Fearon A.E., Grose R.P. Careless talk costs lives: fibroblast growth factor receptor signalling and the consequences of pathway malfunction. Trends Cell Biol 2015; 25(4): 221–233. DOI:10.1016/j.tcb.2014.11.003; Kapp-Simon K.A., Speltz M.L., Cunningham M.L., Patel P.K., Tomita T. Neurodevelopment of children with single suture craniosynostosis: a review. Childs Nerv Syst 2007; 23(3): 269–281. DOI:10.1007/s00381–006–0251-z; https://www.ped-perinatology.ru/jour/article/view/1942

الاتاحة: https://www.ped-perinatology.ru/jour/article/view/1942
https://doi.org/10.21508/1027-4065-2024-69-1-78-85

المؤلفون: Norman A. Saffra, Trisha S. Emborgo, Milan P. Ranka, David S. Kirsch

المصدر: American Journal of Ophthalmology Case Reports, Vol 32, Iss , Pp 101904- (2023)

مصطلحات موضوعية: Myelinated retinal nerve fiber, Crouzon syndrome, MRNF, Increased intracranial pressure, Craniofacial surgery, Ophthalmology, RE1-994

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2451993623001123; https://doaj.org/toc/2451-9936

URL الوصول: https://doaj.org/article/729ec318cb7144e692ff854fa75998be

المؤلفون: Saad Javed, Eesha Yaqoob, Ashraf Mahmood, Bipin Chaurasia

المصدر: International Journal of Medical Arts, Vol 5, Iss 3, Pp 3133-3136 (2023)

مصطلحات موضوعية: crouzon syndrome, hydrocephalous, craniosynostosis, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://ijma.journals.ekb.eg/article_297835_c7f9b287e4e62b9d97561ca0ae6dcf7d.pdf; https://doaj.org/toc/2636-4174; https://doaj.org/toc/2682-3780

URL الوصول: https://doaj.org/article/09d505477bb445f78ef7046af2de6dcc

المؤلفون: Yuling Niu, Jin Xu, Rushan Ye, Zixian Dai, Ling Jin, Wenwen Geng

المصدر: Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-7 (2023)

مصطلحات موضوعية: Strabismus, Crouzon syndrome, Extraocular muscle fibrosis, FGFR2, Genetic, Shallow orbits, Medicine

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1752-1947

URL الوصول: https://doaj.org/article/d477a6a7e6094074a924feb979a000e4

المؤلفون: Sungmi Jeon, Yumin Kim, Ji Hoon Phi, Jee Hyuk Chung

المصدر: Archives of Plastic Surgery, Vol 50, Iss 01, Pp 054-058 (2023)

مصطلحات موضوعية: lefort osteotomy, crouzon syndrome, meningoencephalocele, magnetic resonance imaging, computed tomography, Surgery, RD1-811

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2234-6163; https://doaj.org/toc/2234-6171

URL الوصول: https://doaj.org/article/5827fc47c4cf46819b4a1e8c285b882f

المؤلفون: Juan Guillermo Arámbula Neira, MD, Valeria del Castillo Herazo, MD, Nury Tatiana Rincón Cuenca, MD, Angélica M. Sanabria Cano, MD, Maryi Fernanda Bermudez Sarmiento, MD, María F. Castro, MD, Andrés Felipe Herrera Ortiz, MD

المصدر: Radiology Case Reports, Vol 17, Iss 4, Pp 1288-1292 (2022)

مصطلحات موضوعية: Craniofacial dysostosis, Tomography X-ray computed, Child, Brain diseases, Crouzon syndrome, Craniosynostoses, Medical physics. Medical radiology. Nuclear medicine, R895-920

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S1930043322000589; https://doaj.org/toc/1930-0433

URL الوصول: https://doaj.org/article/4e8fa553f4084963aa05176564ec17d2

المؤلفون: Adriana Lovalho, Augusto de Freitas Barreto, Gustavo Henrique Blumer Astolfi, Alessandra Mazzo, Adriano Yacubian Fernandes

المصدر: Medicina, Vol 56, Iss 1 (2023)

مصطلحات موضوعية: Apert, Crouzon, Neuropsicologia, Testes, Desenvolvimento, Medicine

وصف الملف: electronic resource

Relation: https://www.revistas.usp.br/rmrp/article/view/203361; https://doaj.org/toc/0076-6046; https://doaj.org/toc/2176-7262

URL الوصول: https://doaj.org/article/eb356d801b1e4f36bbdcb01a372afffc

المؤلفون: Kasturi Bhattacharjee, Obaidur Rehman, Vatsalya Venkatraman, Don Kikkawa, Harsha Bhattacharjee, Rahul Gogoi, Aditi Mehta Grewal, Pragya Bhattacharjee

المصدر: Indian Journal of Ophthalmology, Vol 70, Iss 7, Pp 2346-2354 (2022)

مصطلحات موضوعية: craniofacial dysmorphism, craniosynostosis, crouzon, exorbitism, Ophthalmology, RE1-994

وصف الملف: electronic resource

Relation: http://www.ijo.in/article.asp?issn=0301-4738;year=2022;volume=70;issue=7;spage=2346;epage=2354;aulast=Bhattacharjee; https://doaj.org/toc/0301-4738; https://doaj.org/toc/1998-3689

URL الوصول: https://doaj.org/article/042b4e4bb0b64ccb8ff33d6c09a5885c