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23. Solitary angiokeratoma as unusual presentation of Fabry disease: a case report. Ganjei Z; Rahmati R; Panah MY; Meidani FZ; Mosavi A Int J Dermatol; 2023 Jun; 62(6):e346-e348. PubMed ID: 36726172 [No Abstract] [Full Text] [Related]
24. Angiokeratoma regression in a Fabry disease after treatment with agalsidase-beta: clinical effectiveness marker? Fauchais AL; Prey S; Ouatara B; Vidal E; Sparsa A J Eur Acad Dermatol Venereol; 2010 Jun; 24(6):737-8. PubMed ID: 19925601 [No Abstract] [Full Text] [Related]
25. Angiokeratomas - When is a few too many? O'Mahony C; Franks A; Llewellyn R Int J STD AIDS; 2014 Apr; 25(5):378-9. PubMed ID: 24104692 [TBL] [Abstract][Full Text] [Related]
26. DYSPHOSPHOLIPIDOSIS IN FABRY'S DISEASE: A LIGHT AND ELECTRON MICROSCOPIC STUDY. HARTLEY MW; MILLER RE; DEMPSEY HJ; CARROLL JF Ala J Med Sci; 1964 Oct; 1():361-7. PubMed ID: 14227907 [No Abstract] [Full Text] [Related]
27. The renal lesion in angiokeratoma corporis diffusum (Fabry's disease). HENRY EW; RALLY CR Can Med Assoc J; 1963 Aug; 89(5):206-13. PubMed ID: 13953819 [TBL] [Abstract][Full Text] [Related]
30. Misdiagnosis of Fabry disease: importance of biochemical confirmation of clinical or pathological suspicion. Linthorst GE; De Rie MA; Tjiam KH; Aerts JM; Dingemans KP; Hollak CE Br J Dermatol; 2004 Mar; 150(3):575-7. PubMed ID: 15030345 [TBL] [Abstract][Full Text] [Related]
31. [A CASE OF FABRY'S DISEASE WITH SPECIAL REFERENCE TO CHANGES IN THE SKIN, URINARY ALBUMIN, ANHYDROSIS AND KIDNEY FUNCTION]. YOSHITOSHI Y; NAGATA N; NAKAMURA T; MAEDA T Naika; 1965 Mar; 15():555-60. PubMed ID: 14323843 [No Abstract] [Full Text] [Related]
32. Angiokeratoma: a cutaneous marker of Fabry's disease. Albano LM; Rivitti C; Bertola DR; Honjo RS; Kelmann SV; Giugliani R; Kim CA Clin Exp Dermatol; 2010 Jul; 35(5):505-8. PubMed ID: 19843083 [TBL] [Abstract][Full Text] [Related]
33. THE NEUROPATHOLOGY OF HEREDITARY DYSTOPIC LIPIDOSIS. RAHMAN AN; LINDENBERG R Arch Neurol; 1963 Oct; 9():373-85. PubMed ID: 14060085 [No Abstract] [Full Text] [Related]
34. Angiokeratomas, Fabry disease and enzyme replacement therapy: still a challenge. Möhrenschlager M; Henkel V; Ring J Br J Dermatol; 2005 Jan; 152(1):177-8; author reply 178-9. PubMed ID: 15656825 [No Abstract] [Full Text] [Related]
35. Fabry disease and the clinical spectrum of angiokeratomas. Guinovart RM; Bielsa I; Pintos-Morell G; Ferrándiz C Actas Dermosifiliogr; 2013 Apr; 104(3):261-3. PubMed ID: 22975414 [No Abstract] [Full Text] [Related]
36. [Classical type of Fabry disease without angiokeratomas--a case report]. Kudumija B; Mrsić M; Dits S; Matijević V; Thune S; Bozina K Lijec Vjesn; 2007 Dec; 129(12):396-400. PubMed ID: 18383742 [TBL] [Abstract][Full Text] [Related]
37. [Lysosomal storage diseases with angiokeratoma corporis diffusum]. Kanzaki T Nihon Rinsho; 1995 Dec; 53(12):3062-7. PubMed ID: 8577059 [TBL] [Abstract][Full Text] [Related]
38. Multicentric study on the diagnosis of Fabry's disease using angiokeratoma biopsy registries. Kelmann SV; Quaio CR; Honjo RS; Bertola DR; Rosa Neto NS; Lourenço CM; d'Almeida V; Lellis RF; Rivitti-Machado MC; Enokihara MM; Michalany NS; Kim CA Int J Dermatol; 2015 Jun; 54(6):e241-4. PubMed ID: 25778427 [No Abstract] [Full Text] [Related]
39. [CIRCUMSCRIBED ANGIOKERATOMA CORPORIS OF FABRY]. SOTO Actas Dermosifiliogr; 1963; 54():112-3. PubMed ID: 14075951 [No Abstract] [Full Text] [Related]
40. [Mild formes of angiokeratoma corporis diffusion Fabry. On two cases associated with a nevocarcinoma (author's transl)]. Vidmar B; Olmos L; Posternak F; Laugier P Schweiz Rundsch Med Prax; 1977 Jan; 66(1):4-10. PubMed ID: 401998 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]