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637 related items for PubMed ID: 16788417
21. [Audiological findings and mitochondrial DNA mutation in a large family with matrilineal sensorineural hearing loss]. Xing G, Bu X, Yan M, Lu L, Yang S. Zhonghua Er Bi Yan Hou Ke Za Zhi; 2000 Apr; 35(2):98-101. PubMed ID: 12768662 [Abstract] [Full Text] [Related]
22. Nonsyndromic hearing loss caused by a mitochondrial T7511C mutation. Ishikawa K, Tamagawa Y, Takahashi K, Kimura H, Kusakari J, Hara A, Ichimura K. Laryngoscope; 2002 Aug; 112(8 Pt 1):1494-9. PubMed ID: 12172268 [Abstract] [Full Text] [Related]
24. Audiometric analysis of a Belgian family linked to the DFNA10 locus. Verstreken M, Declau F, Schatteman I, Van Velzen D, Verhoeven K, Van Camp G, Willems PJ, Kuhweide EW, Verhaert E, D'Haese P, Wuyts FL, Van de Heyning PH. Am J Otol; 2000 Sep; 21(5):675-81. PubMed ID: 10993457 [Abstract] [Full Text] [Related]
25. Search for mitochondrial DNA mutation at position 3243 in German patients with a positive family history of maternal diabetes mellitus. Klemm T, Neumann S, Trülzsch B, Pistrosch F, Hanefeld M, Paschke R. Exp Clin Endocrinol Diabetes; 2001 Sep; 109(5):283-7. PubMed ID: 11507652 [Abstract] [Full Text] [Related]
26. [A new subtype of diabetes mellitus: maternally inherited diabetes and deafness (MIDD)]. Maassen JA, Jansen JJ, van den Ouweland JM, Hart LM, van Essen EH, Lemkes HH. Ned Tijdschr Geneeskd; 1998 Jan 31; 142(5):229-33. PubMed ID: 9557035 [Abstract] [Full Text] [Related]
27. Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family. Weegerink NJ, Huygen PL, Schraders M, Kremer H, Pennings RJ, Kunst HP. Hear Res; 2011 Dec 31; 282(1-2):167-77. PubMed ID: 21893181 [Abstract] [Full Text] [Related]
36. Deafness due to A1555G mitochondrial mutation without use of aminoglycoside. Matsunaga T, Kumanomido H, Shiroma M, Ohtsuka A, Asamura K, Usami S. Laryngoscope; 2004 Jun 02; 114(6):1085-91. PubMed ID: 15179218 [Abstract] [Full Text] [Related]