Benign hereditary intraepithelial dyskeratosis. Study of a family nucleus
Gombos, F.; Ruocco, V.; Satriano, R.A.
Giornale Italiano di Dermatologia e Venereologia Organo Ufficiale Societa Italiana di Dermatologia e Sifilografia 121(2): 97-101
1986
ISSN/ISBN: 0392-0488 PMID: 3710537 Document Number: 269033
Document emailed within 1 workday
Related Documents
Viprakasit, V.; Tanphaichitr, V.S. 2001: Recurrent A353V mutation in a Thai family with X-linked dyskeratosis congenita Haematologica 86(8): 871-872Calmès, J.M.; Rutz, H.P.; Suardet, L.; Givel, J.C. 1992: Hereditary colorectal cancer: observations of a family study Helvetica Chirurgica Acta 59(2): 349-354
Sturrock, R.R. 1989: A quantitative histological study of the anterodorsal thalamic nucleus and the lateral mammillary nucleus of ageing mice Journal für Hirnforschung 30(2): 191-195
Le-Tkhi-Kuk 1973: Retrograde degeneration of the cells of the oculomotor nucleus (nucleus oculomotorius) following unilateral enucleation of the eye (experimental study) Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 73(1): 50-53
Bonfiglio, T.A.; Patten, S.F. 1976: Histopathologic spectrum of benign proliferative and intraepithelial neoplastic reactions of the uterine cervix Journal of Reproductive Medicine 16(5): 253-262
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
Svendsen, I.H.; Steensgaard-Hansen, F.; Nordvåg, B.Y. 1999: Hereditary amyloid cardiomyopathy related to a mutation at transthyretin protein number 111. a clinical, genetic and echocardiographic study of an affected Danish family Ugeskrift for Laeger 161(36): 4995-4999
Suzuki, H. 1978: Electron microscopic study on the changes of the cerebellar hemisphere cortex and lateral nucleus (dentate nucleus) of adult rats after electric convulsions--changes of astrocytes and purkinje cell perikarya and distal parts of their axons Seishin Shinkeigaku Zasshi 80(3): 105-119
Zhang, G.-s.; Peng, H.-l.; Yi, Y.; Xie, D.-h.; He, X.-b. 2004: Mutation of the activin receptor-like kinase 1(ALK1) gene and the expression of plasma thrombomodulin in type-2 hereditary hemorrhagic telangiectasia: a study of a Chinese family Zhonghua Yi Xue Za Zhi 84(3): 182-185
Sossenheimer, M.J.; Aston, C.E.; Preston, R.A.; Gates, L.K.; Ulrich, C.D.; Martin, S.P.; Zhang, Y.; Gorry, M.C.; Ehrlich, G.D.; Whitcomb, D.C. 1997: Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. the Midwest Multicenter Pancreatic Study Group (MMPSG) American Journal of Gastroenterology 92(7): 1113-1116
Sebastián de Erice, M.; Romero López, J.; Navarro Esteban, J.; Jiménez, F.; Soto Faure, L. 1981: Hereditary optic atrophies. Study of a family with dominant autosomal optic atrophy Revista Clinica Espanola 163(5): 341-343
Abbruzzese, M.; Gatti, R.; Ratto, S.; Bugiani, O. 1978: Hereditary sensory neuropathy with anhidrosis. A new family with a study of the sensory conduction velocity Acta Neurologica 33(5): 413-418
Patel, P.; Nayak, J.G.; Biljetina, Z.; Donnelly, B.; Trpkov, K. 2015: Prostate cancer after initial high-grade prostatic intraepithelial neoplasia and benign prostate biopsy Canadian Journal of Urology 22(6): 8056-8062
Zhang, J.D.; Yang, X.L. 1999: Projections from subnucleus oralis of the spinal trigeminal nucleus to contralateral thalamus via the relay of juxtatrigeminal nucleus and dorsomedial part of the principal sensory trigeminal nucleus in the rat Journal für Hirnforschung 39(3): 301-310
Maygarden, S.J.; Strom, S.; Ware, J.L. 1992: Localization of epidermal growth factor receptor by immunohistochemical methods in human prostatic carcinoma, prostatic intraepithelial neoplasia, and benign hyperplasia Archives of Pathology and Laboratory Medicine 116(3): 269-273
Aaltonen, L.A.; Peltomäki, P.; Mecklin, J.P.; Järvinen, H.; Jass, J.R.; Green, J.S.; Lynch, H.T.; Watson, P.; Tallqvist, G.; Juhola, M. 1994: Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients Cancer Research 54(7): 1645-1648
Yamada, S.; Yamada, R.; Nakamura, M. 1988: Study on mean platelet volume, platelet distribution width, platelet associated IgG in a family with hereditary thrombocytopenia Rinsho Byori. Japanese Journal of Clinical Pathology 36(6): 667-673
Heinzl, S. 1996: Diagnostic and morphologic criteria in cervix intraepithelial neoplasia (CIN) and squamous intraepithelial lesion (SIL) and differentiated therapy Zentralblatt für Gynakologie 118(6): 339-342
Maggwa, B.N.; Hunter, D.J.; Mbugua, S.; Tukei, P.; Mati, J.K. 1993: The relationship between HIV infection and cervical intraepithelial neoplasia among women attending two family planning clinics in Nairobi, Kenya Aids 7(5): 733-738
Tan, C.T. 1980: A family with hereditary ataxia Medical Journal of Malaysia 35(2): 134-138