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Anosmia and Ageusia in Parkinson's Disease.
More on X-linked ichthyosis, steroid sulfatase deficiency, and hypogonadism and anosmia.
X-linked ichthyosis due to steroid sulfatase deficiency associated with hypogonadism and anosmia.
Brain perfusion single photon emission computed tomography findings in patients with posttraumatic anosmia and comparison with radiological imaging.
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse.
X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome.
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules.
Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome.
Clinical assessment and genomic landscape of a consanguineous family with three Kallmann syndrome descendants.
Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome.
Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson's disease.
Impairment of olfactory recognition after closed head injury.
Lewy bodies and olfactory dysfunction in old age.
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