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Brain Changes in Kallmann Syndrome
BACKGROUND AND PURPOSE: Kallmann syndrome is a rare inherited disorder due to defective intrauterine migration of olfactory axons and gonadotropin-releasing hormone neurons, leading to rhinencephalon hypoplasia and hypogonadotropic hypogonadism. Concomitant brain developmental abnormalities have bee...
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| Publicado no: | AJNR Am J Neuroradiol |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Neuroradiology
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7966280/ https://ncbi.nlm.nih.gov/pubmed/24788131 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A3946 |
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