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129 related items for PubMed ID: 10925376
1. Kallmann syndrome in three unrelated women and an association with femur-fibula-ulna dysostosis in one case. Gasztonyi Z, Barsi P, Czeizel AE. Am J Med Genet; 2000 Jul 31; 93(3):176-80. PubMed ID: 10925376 [Abstract] [Full Text] [Related]
8. Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients. Sato N, Katsumata N, Kagami M, Hasegawa T, Hori N, Kawakita S, Minowada S, Shimotsuka A, Shishiba Y, Yokozawa M, Yasuda T, Nagasaki K, Hasegawa D, Hasegawa Y, Tachibana K, Naiki Y, Horikawa R, Tanaka T, Ogata T. J Clin Endocrinol Metab; 2004 Mar 31; 89(3):1079-88. PubMed ID: 15001591 [Abstract] [Full Text] [Related]
9. [A case of Kallmann syndrome: diagnostic usefulness of cranial magnetic resonance imaging]. Shiraishi K, Naito K. Hinyokika Kiyo; 2000 Jul 31; 46(7):509-12. PubMed ID: 10965462 [Abstract] [Full Text] [Related]
11. [Olfactory function and olfactory bulbs in patients with Kallmann syndrome]. Kokoreva KD, Chugunov IS, Vladimirova VP, Ivannikova TE, Bogdanov VP, Bezlepkina OB. Probl Endokrinol (Mosk); 2023 May 11; 69(2):67-74. PubMed ID: 37448273 [Abstract] [Full Text] [Related]
12. Reconsidering olfactory bulb magnetic resonance patterns in Kallmann syndrome. Hacquart T, Ltaief-Boudrigua A, Jeannerod C, Hannoun S, Raverot G, Pugeat M, Brac de la Perriere A, Lapras V, Nugues F, Dode C, Cotton F. Ann Endocrinol (Paris); 2017 Oct 11; 78(5):455-461. PubMed ID: 28807454 [Abstract] [Full Text] [Related]
13. [Femur-fibula-ulna (FFU) complex in the 33rd week of gestation: ultrasonography, radiology, pathology and differential diagnosis. Case report]. Guschmann M, Becker R, Urban M, Entezami M, Hese S, Vogel M. Klin Padiatr; 2001 Oct 11; 213(5):301-5. PubMed ID: 11582532 [Abstract] [Full Text] [Related]
14. MR evaluation of patients with congenital hyposmia or anosmia. Yousem DM, Geckle RJ, Bilker W, McKeown DA, Doty RL. AJR Am J Roentgenol; 1996 Feb 11; 166(2):439-43. PubMed ID: 8553963 [Abstract] [Full Text] [Related]
15. Kallmann syndrome in an adolescent boy. Jana M, Kumar A. Pediatr Radiol; 2010 Dec 11; 40 Suppl 1():S164. PubMed ID: 20224965 [No Abstract] [Full Text] [Related]
16. The femur, fibula, ulna (FFU) complex in siblings. Zlotogora J, Rosenmann E, Menashe M, Robin GC, Cohen T. Clin Genet; 1983 Dec 11; 24(6):449-52. PubMed ID: 6652959 [Abstract] [Full Text] [Related]
17. Kallmann syndrome: MR findings. Knorr JR, Ragland RL, Brown RS, Gelber N. AJNR Am J Neuroradiol; 1993 Dec 11; 14(4):845-51. PubMed ID: 8352155 [Abstract] [Full Text] [Related]
18. Case report: olfactory function in a fertile eunuch with Kallmann syndrome. Wortsman J, Hughes LF. Am J Med Sci; 1996 Mar 11; 311(3):135-8. PubMed ID: 8615388 [Abstract] [Full Text] [Related]
19. [Neuroradiology of Kallmann's syndrome]. de m Freitas P, Carvalho S, Ribeiro F, Marnoto D, Martins F. Acta Med Port; 2001 Mar 11; 14(1):123-6. PubMed ID: 11321967 [Abstract] [Full Text] [Related]
20. Mutation analyses in pedigrees and sporadic cases of ethnic Han Chinese Kallmann syndrome patients. Gu WJ, Zhang Q, Wang YQ, Yang GQ, Hong TP, Zhu DL, Yang JK, Ning G, Jin N, Chen K, Zang L, Wang AP, Du J, Wang XL, Yang LJ, Ba JM, Lv ZH, Dou JT, Mu YM. Exp Biol Med (Maywood); 2015 Nov 11; 240(11):1480-9. PubMed ID: 26031747 [Abstract] [Full Text] [Related] Page: [Next] [New Search]