共 143 条
[1]
Cariboni A(2006)Kallmann’s syndrome, a neuronal migration defect Cell Mol Life Sci 63 2512-2526
[2]
Maggi R(2003)Kallmann’s syndrome: molecular pathogenesis Int J Biochem Cell Biol 35 1157-1162
[3]
Hu Y(2001)The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics J Clin Endocrinol Metab 86 1532-1538
[4]
Tanriverdi F(2008)The complex genetics of Kallmann syndrome: KALI, FGFR1, FGF8, PROKR2, PROK2, et al Sex Dev 2 181-193
[5]
MacColl GS(2004)Kallmann syndrome: fibroblast growth factor signaling insufficiency? J Mol Med (Berl) 82 725-734
[6]
Bouloux PM(2008)Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome Am J Hum Genet 83 511-519
[7]
Oliveira LM(2012)SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome PLoS Genet 8 e1002896-122
[8]
Seminara SB(2010)Immunohistochemical, volumetric, and functional neuroimaging studies in patients with idiopathic Parkinson’s disease J Neurol Sci 289 119-543
[9]
Beranova M(2009)Olfactory-induced brain activity in Parkinson’s disease relates to the expression of event-related potentials: a functional magnetic resonance imaging study Neuroscience 162 537-181
[10]
Hardelin JP(2010)Smell and preclinical Alzheimer disease: study of 29 patients with amnesic mild cognitive impairment J Otolaryngol Head Neck Surg 39 175-841