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22. Congenital insensitivity to pain--review and report of a case with dental implications. Butler J; Fleming P; Webb D Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2006 Jan; 101(1):58-62. PubMed ID: 16360608 [TBL] [Abstract][Full Text] [Related]
23. Congenital indifference to pain. Khan SA; Peterkin GA Trans St Johns Hosp Dermatol Soc; 1970; 56(2):122-30. PubMed ID: 4102596 [No Abstract] [Full Text] [Related]
24. Sensory phenotype assessment in a young girl affected by congenital insensitivity to pain (CIPA). Bachiocco V; Bergamaschi R; Mondardini MC; Bronzetti G Paediatr Anaesth; 2007 Nov; 17(11):1105-10. PubMed ID: 17897279 [TBL] [Abstract][Full Text] [Related]
25. Neurophysiological study in an Italian family with autosomal dominant late-onset leukodystrophy. Leombruni S; Vaula G; Coletti Moja M; Bergui M; Bergamini L; Quattrocolo G Electromyogr Clin Neurophysiol; 1998; 38(3):131-5. PubMed ID: 9637937 [TBL] [Abstract][Full Text] [Related]
27. Hereditary pancreatitis--a case report. Braulke I; Zoll B; Hartmann H Z Gastroenterol; 1994 Nov; 32(11):645-6. PubMed ID: 7886974 [TBL] [Abstract][Full Text] [Related]
28. [Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary transmission based on the analysis of a 3-generation family tree]. De Marchi S; Proto G; Jengo A; Collinassi P; Basile A Minerva Med; 1983 Feb; 74(7):301-6. PubMed ID: 6828258 [TBL] [Abstract][Full Text] [Related]
34. [Pattern ERG and pattern visually evoked cortical potentials in autosomal dominant infantile optic atrophy]. Papst N; Bopp M; Wundrack EM Fortschr Ophthalmol; 1985; 82(3):300-1. PubMed ID: 4029857 [No Abstract] [Full Text] [Related]
35. Hereditary glaucoma: a report of two pedigrees. Lee DA; Brubaker RF; Hruska L Ann Ophthalmol; 1985 Dec; 17(12):739-41. PubMed ID: 4091373 [TBL] [Abstract][Full Text] [Related]
37. [Congenital indifference to pain, apropos of a case with antecedents of consanguinity]. Guillermo A; Grinspan A Rev Neurol (Paris); 1970 Dec; 123(6):434-5. PubMed ID: 4105227 [No Abstract] [Full Text] [Related]
38. Phenotype and counseling in lacrimo-auriculo-dento-digital (LADD) syndrome. Horn D; Witkowski R Genet Couns; 1993; 4(4):305-9. PubMed ID: 8110420 [TBL] [Abstract][Full Text] [Related]
39. Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom. Warner TT; Lennox GG; Janota I; Harding AE Mov Disord; 1994 May; 9(3):289-96. PubMed ID: 8041369 [TBL] [Abstract][Full Text] [Related]
40. Tetrasomy 18p: a distinctive syndrome. Rivera H; Möller M; Hernández A; Enríquez-Guerra MA; Arreola R; Cantú JM Ann Genet; 1984; 27(3):187-9. PubMed ID: 6334486 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]