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neonatal wide cranial sutures相关文献:
Yunis Varon syndrome.
Kulkarni ML, Vani HN, Nagendra K, Mahesh TK, Kumar A, Haneef S, Mohammed Z, Kulkarni PM.
Indian J Pediatr. 2006 Apr;73(4):353-5. doi: 10.1007/BF02825832.
PMID:16816498
Wide sutures and large fontanels in the newborn.
Tan KL.
Am J Dis Child. 1976 Apr;130(4):386-90. doi: 10.1001/archpedi.1976.02120050044007.
PMID:1266823
Hypophosphatasia in a newborn infant.
Tekinalp G, Yükselen A, Balkanci F, Coşkun T, Yurdakök M.
Turk J Pediatr. 1995 Jan-Mar;37(1):61-5.
PMID:7732610
Subtotal neonatal calvariectomy for severe craniosynostosis.
Hanson JW, Sayers MP, Knopp LM, Macdonald C, Smith DW.
J Pediatr. 1977 Aug;91(2):257-60. doi: 10.1016/s0022-3476(77)80823-8.
PMID:889596
A monoallelic SEC23A variant E599K associated with cranio-lenticulo-sutural dysplasia.
Cisarova K, Garavelli L, Caraffi SG, Peluso F, Valeri L, Gargano G, Gavioli S, Trimarchi G, Neri A, Campos-Xavier B, Superti-Furga A.
Am J Med Genet A. 2022 Jan;188(1):319-325. doi: 10.1002/ajmg.a.62506. Epub 2021 Sep 28.
PMID:34580982
A review of hedgehog signaling in cranial bone development.
Pan A, Chang L, Nguyen A, James AW.
Front Physiol. 2013 Apr 2;4:61. doi: 10.3389/fphys.2013.00061. eCollection 2013.
PMID:23565096
Craniosynostosis: prenatal diagnosis by means of ultrasound and SSSE-MRI. Family series with report of neurodevelopmental outcome and review of the literature.
Tonni G, Panteghini M, Rossi A, Baldi M, Magnani C, Ferrari B, Lituania M.
Arch Gynecol Obstet. 2011 Apr;283(4):909-16. doi: 10.1007/s00404-010-1643-6. Epub 2010 Sep 2.
PMID:20811900
An unusually-wide human bregmatic Wormian bone: anatomy, tomographic description, and possible significance.
Barberini F, Bruner E, Cartolari R, Franchitto G, Heyn R, Ricci F, Manzi G.
Surg Radiol Anat. 2008 Nov;30(8):683-7. doi: 10.1007/s00276-008-0371-0. Epub 2008 Jun 4.
PMID:18523715
3C syndrome: third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome).
Verloes A, Dresse MF, Jovanovic M, Dodinval P, Geubelle F.
Clin Genet. 1989 Mar;35(3):205-8. doi: 10.1111/j.1399-0004.1989.tb02929.x.
PMID:2650935
Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?
Faria ÁC, Rabbi-Bortolini E, Rebouças MRGO, de S Thiago Pereira ALA, Frasson MGT, Atique R, Lourenço NCV, Rosenberg C, Kobayashi GS, Passos-Bueno MR, Errera FIV.
Am J Med Genet A. 2016 Feb;170A(2):403-409. doi: 10.1002/ajmg.a.37448. Epub 2015 Nov 14.
PMID:26566760
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