Hereditary pachyonychia
Somov, B.A.; Khamaganova, A.V.; Bogomil'skaia, M.A.
Sovetskaia Meditsina 36(9): 147-148
1973
ISSN/ISBN: 0038-5077 PMID: 4801382 Document Number: 66383
Document emailed within 1 workday
Related Documents
Paller, A.S.; Moore, J.A.; Scher, R. 1991: Pachyonychia congenita tarda. a late-onset form of pachyonychia congenita Archives of Dermatology 127(5): 701-703Van Steensel, M.A.; Smith, F.J.; Steijlen, P.M. 2001: A new type of pachyonychia congenita European Journal of Dermatology: Ejd 11(3): 188-190
Ginter, E.K.; Budagova, K.A.; Revazov, A.A.; Petrin, A.N.; Bugaeva, E.A. 1986: Medico-genetical study of the Uzbekistan population. IX. Variability of hereditary pathology, territorial distribution of hereditary diseases and hereditary disease load in the population of the Urgut district of the Samarkand region Genetika 22(7): 1199-1206
Hodes, M.E.; Norins, A.L. 1977: Pachyonychia congenita and steatocystoma multiplex Clinical Genetics 11(5): 359-364
Kohli, N. 2009: Pachyonychia congenita: a case report Cutis 84(5): 269-271
Egorov, N.A.; Golychev, V.N. 1980: Lesion of the eyes in congenital pachyonychia Vestnik Oftalmologii 4: 66-67
Forslind, B.; Nylén, B.; Swanbeck, G.; Thyresson, M.; Thyresson, N. 1973: Pachyonychia congenita. a histologic and microradiographic study Acta Dermato-Venereologica 53(3): 211-216
Rondón Lugo, A.J. 1982: Congenital pachyonychia treated by oral retinoid Medicina Cutanea Ibero-Latino-Americana 10(6): 395-398
Cammarata-Scalisi, F.; Natsuga, K.; Toyonaga, E.; Nishie, W.; Shimizu, H.; Stock, F.; Milano, M.; Petrosino, P.; Arenas de Sotolongo, A.; Medina, Y. 2015: Clinical and molecular findings of pachyonychia congenita type 2 (PC-2) Gaceta Medica de Mexico 151(2): 270-272
Dupré, A.; Christol, B.; Bonafé, J.L.; Touron, P. 1981: Pachyonychia congenita. Three familial cases. Effects of the treatment by aromatic retinoid (RO 10.9359) Annales de Dermatologie et de Venereologie 108(2): 145-149
Nørby, S.; Rosenberg, T. 1990: Leber's hereditary optic atrophy. a hereditary disease caused by mitochondrial DNA mutation Ugeskrift for Laeger 152(43): 3149-3152
Nüssli, R. 1971: Growth of patients with hereditary fructose intolerance or hereditary saccharose-isomaltose malabsorption Helvetica Paediatrica Acta 26(5): 637-647
Vanderstock, L.; Vander Eecken, P.; Vermeersch, H. 1983: Hereditary angioedema. A hereditary disorder in the synthesis of the complement system Acta Oto-Rhino-Laryngologica Belgica 36(3): 418-431
Cardinali, C.; Torchia, D.; Caproni, M.; Petrini, N.; Fabbri, P. 2004: Case study: pachyonychia congenita: a mixed type II-type IV presentation Skinmed 3(4): 233-235
Sevilla, T. 2000: The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies Revista de Neurologia 30(1): 71-79
Bélanger, L.; Bélanger, M.; Prive, L.; Larochelle, J.; Tremblay, M.; Aubin, G. 1973: Hereditary tyrosinemia and alpha-1-fetoprotein. I. Clinical value of alpha-fetoprotein in hereditary tyrosinemia Pathologie-Biologie 21(5): 449-455
Kirkels, V.G.; Vemer, H.M.; Hamel, B.C. 1988: Hereditary, what does it mean? Nederlands Tijdschrift Voor Geneeskunde 132(50): 2265-2267
Mano, T. 1971: Hereditary ataxia Nihon Rinsho. Japanese Journal of Clinical Medicine 29(8): 1897-1906
Rosenberg, T. 1989: Hereditary eye diseases Ugeskrift for Laeger 151(12): 791-794
Schorderet, D.F. 1996: Hereditary cancers Praxis 85(35): 1017-1018