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