These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
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 [No Abstract] [Full Text] [Related]
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 [No Abstract] [Full Text] [Related]
68. [Coats retinitis and retinal angiomatosis]. BEAUVIEUX, CLAVEL. Arch Ophtalmol Rev Gen Ophtalmol; 1946 Mar 15; 6(2):189. PubMed ID: 21064963 [No Abstract] [Full Text] [Related]
70. Letter: Marshall syndrome: eulogy or resurrection? Zellweger H. J Pediatr; 1975 May 15; 86(5):817. PubMed ID: 1133671 [No Abstract] [Full Text] [Related]
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 [No Abstract] [Full Text] [Related]
72. [Coats' retinitis; clinical, anatomopathological, etiogenetic contribution]. SCUDERI G. Ann Ottalmol Clin Ocul; 1951 Jan 15; 77(1):21-37. PubMed ID: 14819825 [No Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]