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PUBMED FOR HANDHELDS

Journal Abstract Search


112 related items for PubMed ID: 3402627

  • 61. 'Atrichosis', a new hairless gene with cyst formation in rats.
    Ohno T, Yoshida H.
    Experientia; 1981 Feb 15; 37(2):126-7. PubMed ID: 7238735
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  • 63. Digestive tract and renal small vessel hyalinosis, idiopathic nonarteriosclerotic intracerebral calcifications, retinal ischemic syndrome, and phenotypic abnormalities. A new familial syndrome.
    Rambaud JC, Galian A, Touchard G, Morel-Maroger L, Mikol J, Van Effenterre G, Leclerc JP, Le Charpentier Y, Haut J, Matuchansky C.
    Gastroenterology; 1986 Apr 15; 90(4):930-8. PubMed ID: 3485063
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  • 67. The destruction of retinal angiomas by diathermy.
    LEWIS PM.
    J Tn State Med Assoc; 1949 Mar 15; 42(3):75-8. PubMed ID: 18112590
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  • 68. [Coats retinitis and retinal angiomatosis].
    BEAUVIEUX, CLAVEL.
    Arch Ophtalmol Rev Gen Ophtalmol; 1946 Mar 15; 6(2):189. PubMed ID: 21064963
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  • 70. Letter: Marshall syndrome: eulogy or resurrection?
    Zellweger H.
    J Pediatr; 1975 May 15; 86(5):817. PubMed ID: 1133671
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  • 71. A case report of two siblings with familial leukoencephalopathy in normotensive male adults with alopecia and lumbago.
    Miyaoka H, Sakai T, Kamijima K, Kato Y, Hoshino H, Kim Y.
    Int J Geriatr Psychiatry; 1998 Sep 15; 13(9):643-4. PubMed ID: 9777431
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  • 72. [Coats' retinitis; clinical, anatomopathological, etiogenetic contribution].
    SCUDERI G.
    Ann Ottalmol Clin Ocul; 1951 Jan 15; 77(1):21-37. PubMed ID: 14819825
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  • 76. Multisystemic Manifestations in Rare Diseases: The Experience of Dyskeratosis Congenita.
    Callea M, Martinelli D, Cammarata-Scalisi F, Grimaldi C, Jilani H, Grimaldi P, Willoughby CE, Morabito A.
    Genes (Basel); 2022 Mar 11; 13(3):. PubMed ID: 35328050
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  • 77. Leukoencephalopathy with brain calcifications and cysts (Labrune syndrome) case report: diagnosis and management of a rare neurological disease.
    Paff M, Samuel N, Alsafwani N, Paul D, Diamandis P, Climans SA, Kucharczyk W, Ding MYR, Gao AF, Lozano AM.
    BMC Neurol; 2022 Jan 05; 22(1):10. PubMed ID: 34986804
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  • 78. Disease progression and clinical outcomes in telomere biology disorders.
    Niewisch MR, Giri N, McReynolds LJ, Alsaggaf R, Bhala S, Alter BP, Savage SA.
    Blood; 2022 Mar 24; 139(12):1807-1819. PubMed ID: 34852175
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  • 79. Novel compound heterozygous STN1 variants are associated with Coats Plus syndrome.
    Acharya T, Firth HV, Dugar S, Grammatikopoulos T, Seabra L, Walters A, Crow YJ, Parker APJ.
    Mol Genet Genomic Med; 2021 Dec 24; 9(12):e1708. PubMed ID: 34110109
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