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62. Unique cerebellar-cerebral form of autosomal recessive ataxia. Matsubara E; Nagata T; Kageyama Y; Shiote M; Namba R; Nagano I; Shoji M; Abe K Tohoku J Exp Med; 2005 Sep; 207(1):81-5. PubMed ID: 16082159 [TBL] [Abstract][Full Text] [Related]
63. Localized forms of steatocystoma multiplex: case report and review of the literature. Mortazavi H; Taheri A; Mansoori P; Kani ZA Dermatol Online J; 2005 Mar; 11(1):22. PubMed ID: 15748563 [TBL] [Abstract][Full Text] [Related]
64. [A case of cerebral gigantism with cerebellar atrophy]. Kitazawa K; Ikeda M; Tsukagoshi H Rinsho Shinkeigaku; 1990 May; 30(5):520-3. PubMed ID: 2401112 [TBL] [Abstract][Full Text] [Related]
65. Steatocystoma simplex in penile foreskin: a case report. de Lima MM; de Lima MM; Granja F J Med Case Rep; 2016 Mar; 10():49. PubMed ID: 26951088 [TBL] [Abstract][Full Text] [Related]
66. Autosomal dominant cerebellar ataxia (SCA6): clinical, genetic and neuropathological study in a family. Takahashi H; Ikeuchi T; Honma Y; Hayashi S; Tsuji S Acta Neuropathol; 1998 Apr; 95(4):333-7. PubMed ID: 9560009 [TBL] [Abstract][Full Text] [Related]
67. Familial hypobeta-lipoproteinemia: studies in 13 kindreds. Glueck CJ; Gartside PS; Mellies MJ; Steiner PM Trans Assoc Am Physicians; 1977; 90():184-203. PubMed ID: 205980 [No Abstract] [Full Text] [Related]
68. [Central pontine myelinolysis with cerebellar ataxia and dystonia]. Gille M; Jacquemin C; Kiame G; Delbecq J; Guilmot D; Depré A Rev Neurol (Paris); 1993; 149(5):344-6. PubMed ID: 8272731 [TBL] [Abstract][Full Text] [Related]
69. CO2 laser therapy for steatocystoma multiplex. Krähenbühl A; Eichmann A; Pfaltz M Dermatologica; 1991; 183(4):294-6. PubMed ID: 1809593 [TBL] [Abstract][Full Text] [Related]
70. [Persistent cerebellar ataxia following typhoid fever]. Inoue H; Nishinaka K; Urushitani M; Udaka F; Kameyama M Rinsho Shinkeigaku; 1995 Oct; 35(10):1151-4. PubMed ID: 8821502 [TBL] [Abstract][Full Text] [Related]
73. Subacute cerebellar ataxia and atrophy developed in a young woman with systemic lupus erythematosus whose cerebrospinal fluid was positive for antineuronal cell antibody. Iwasaki Y; Okamoto A; Shoda H; Takahashi Y; Fujio K; Kawahata K; Yamamoto K Lupus; 2012 Mar; 21(3):324-8. PubMed ID: 21965279 [TBL] [Abstract][Full Text] [Related]
74. Congenital linear steatocystoma multiplex of the nose. Park YM; Cho SH; Kang H Pediatr Dermatol; 2000; 17(2):136-8. PubMed ID: 10792805 [TBL] [Abstract][Full Text] [Related]
75. Genetic analysis of a kindred with familial hypobetalipoproteinemia. Evidence for two separate gene defects: one associated with an abnormal apolipoprotein B species, apolipoprotein B-37; and a second associated with low plasma concentrations of apolipoprotein B-100. Young SG; Bertics SJ; Curtiss LK; Dubois BW; Witztum JL J Clin Invest; 1987 Jun; 79(6):1842-51. PubMed ID: 3473077 [TBL] [Abstract][Full Text] [Related]
76. Cerebellar atrophy in a patient with anorexia nervosa. Miwa H; Nakanishi I; Kodama R; Kondo T Int J Eat Disord; 2004 Sep; 36(2):238-41. PubMed ID: 15282696 [TBL] [Abstract][Full Text] [Related]
77. Eruptive vellus hair cyst and steatocystoma multiplex: hybrid cysts. Hurlimann AF; Panizzon RG; Burg G Dermatology; 1996; 192(1):64-6. PubMed ID: 8832957 [TBL] [Abstract][Full Text] [Related]
78. A simple surgical technique for the treatment of steatocystoma multiplex. Kaya TI; Ikizoglu G; Kokturk A; Tursen U Int J Dermatol; 2001 Dec; 40(12):785-8. PubMed ID: 11903679 [TBL] [Abstract][Full Text] [Related]
79. Liver fibrosis in a patient with familial homozygous hypobetalipoproteinaemia: possible role of vitamin supplementation. Scoazec JY; Bouma ME; Roche JF; Blache D; Verthier N; Feldmann G; Gay G Gut; 1992 Mar; 33(3):414-7. PubMed ID: 1568667 [TBL] [Abstract][Full Text] [Related]
80. [Cerebellar ataxia due to hypothyroidism in adults (case report)]. Hammar CH; Regli F Dtsch Med Wochenschr; 1975 Jul; 100(28):1504-6. PubMed ID: 1137948 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]