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Journal Abstract Search
113 related items for PubMed ID: 11819074
1. Proboscis lateralis: radiological evaluation. Belet N, Belet U, Tekat A, Küçüködük U. Pediatr Radiol; 2002 Feb; 32(2):99-101. PubMed ID: 11819074 [Abstract] [Full Text] [Related]
2. Proboscis lateralis with ipsilateral sinonasal and olfactory pathway aplasia. Vaid S, Shah D, Rawat S, Shukla R. J Pediatr Surg; 2010 Feb; 45(2):453-6. PubMed ID: 20152374 [Abstract] [Full Text] [Related]
3. Neuromuscular hamartoma: imaging features of a rare paediatric craniofacial tumour. Oeppen RS, Harden SP, Argent JD. Pediatr Radiol; 2003 Jan; 33(1):50-2. PubMed ID: 12497240 [Abstract] [Full Text] [Related]
4. Proboscis lateralis: case report and review. Thorne MC, Ruiz RE, Carvalho J, Lesperance MM. Arch Otolaryngol Head Neck Surg; 2007 Oct; 133(10):1051-3. PubMed ID: 17938331 [No Abstract] [Full Text] [Related]
5. Proboscis lateralis-like appendage: description of a new facial anomaly. Arora G, Arora V, Chawla D. Ann Plast Surg; 2011 Apr; 66(4):357-9. PubMed ID: 21200312 [Abstract] [Full Text] [Related]
6. Craniofacial characteristics evidenced in Bartsocas-Papas syndrome from birth to five years. Case report. Maganzini AL, Rios A, Shanske A. N Y State Dent J; 2006 Apr; 72(4):34-7. PubMed ID: 16925011 [Abstract] [Full Text] [Related]
7. Intracranial and extracranial malformations in patients with craniofacial anomalies. Tunçbilek G, Alanay Y, Uzun H, Kayikçioğlu A, Akarsu NA, Benli K. J Craniofac Surg; 2010 Sep; 21(5):1460-4. PubMed ID: 20818260 [Abstract] [Full Text] [Related]
8. [Medial cleft lip: one diagnosis masking another]. Mansouri Hattab N, Lahmiti S, Bouaichi A, Hiroual A, El Bouihi M, Fikry T. Arch Pediatr; 2011 Feb; 18(2):149-52. PubMed ID: 21194907 [Abstract] [Full Text] [Related]
9. Alobar holoprosencephaly associated with cebocephaly and craniosynostosis. Lin CH, Tsai JD, Ho YJ, Lin WC. Acta Neurol Taiwan; 2009 Jun; 18(2):123-6. PubMed ID: 19673365 [Abstract] [Full Text] [Related]
10. Lissencephaly: diagnosis by computed tomography and magnetic resonance imaging. Cordes M, Cordes I, Sander B, Sperner J, Hedde JP. Eur J Radiol; 1988 May; 8(2):131-3. PubMed ID: 3383858 [Abstract] [Full Text] [Related]
12. Acro-cardio-facial syndrome associated with neuroepithelial cyst: a case report. Sivasli O, Ozer EA, Ozer A, Aydinlioglu H, Helvaci M. Genet Couns; 2007 May; 18(2):247-50. PubMed ID: 17710878 [Abstract] [Full Text] [Related]
13. MRI findings in macrocephaly-cutis marmorata telangiectatica congenita. Carcao M, Blaser SI, Grant RM, Weksberg R, Siegel-Bartelt J. Am J Med Genet; 1998 Mar 05; 76(2):165-7. PubMed ID: 9511980 [Abstract] [Full Text] [Related]
14. Craniofacial duplication (diprosopus): CT, MR imaging, and MR angiography findings case report. Hähnel S, Schramm P, Hassfeld S, Steiner HH, Seitz A. Radiology; 2003 Jan 05; 226(1):210-3. PubMed ID: 12511692 [Abstract] [Full Text] [Related]
15. Coexistence of proboscis lateralis and multiple craniofacial, neurological, cardiac and spinal deformities: a one-of-a-kind case report. Zaidi AK, Arif A, Butt M, Tebha SS, Ray I, Yosufi A, Dehgani-Mobaraki P. BMC Pediatr; 2023 Feb 10; 23(1):70. PubMed ID: 36759785 [Abstract] [Full Text] [Related]
16. [Fryns syndrome. Report on 3 new cases]. Alessandri JL, Attali T, Brayer C, Dupuy L, Pilorget H, Ramful D, Samperiz S, Tiran-Rajaofera I, Robin S. Arch Pediatr; 2007 Jul 10; 14(7):903-7. PubMed ID: 17442547 [Abstract] [Full Text] [Related]
18. MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literature. Garavelli L, Leask K, Zanacca C, Pedori S, Albertini G, Della Giustina E, Croci GF, Magnani C, Banchini G, Clayton-Smith J, Bocian M, Firth H, Gold JA, Hurst J. Genet Couns; 2005 Feb 10; 16(2):117-28. PubMed ID: 16080291 [Abstract] [Full Text] [Related]
19. Maxillary intraosseous vascular malformation: a case report and literature review. Naraghi A, Keene M. J Laryngol Otol; 2007 Apr 10; 121(4):404-7. PubMed ID: 17403266 [Abstract] [Full Text] [Related]
20. Choroid plexus hyperplasia and monosomy 1p36: report of new findings. Puvabanditsin S, Garrow E, Patel N, D'Elia A, Zaafran A, Phattraprayoon N, Davis SE. J Child Neurol; 2008 Aug 10; 23(8):922-5. PubMed ID: 18660475 [Abstract] [Full Text] [Related] Page: [Next] [New Search]