Kallmann syndrome and deafness: an uncommon combination: A case report and a literature review
, 2016 Nader Salama
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A familial case of Kallmann syndrome: novel variants in ANOS1 and GNRHR genes. [PDF]
Arch Endocrinol MetabPacheco ALP +5 more
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A rare case of a 34-year-old patient diagnosed late with Kallmann syndrome: case report. [PDF]
Pan Afr Med J, 2022 Aristiady EB, Alberta D.
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Mutation spectrum and frequency of copy number variations of the ANOS1 gene in patients with Kallmann syndrome or normosmic isolated hypogonadotropic hypogonadism. [PDF]
Endocr Connect, 2023 Hye Kim J +8 more
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Prioritizing Genetic Testing in Patients With Kallmann Syndrome Using Clinical Phenotypes [PDF]
, 2013 Flavia Amanda Costa‐Barbosa +15 more
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Altered glucose metabolism in default mode network and prefrontal circuit in patients with Kallmann syndrome. [PDF]
EJNMMI ResZhou C +8 more
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Molecular diagnosis of Kallmann syndrome with diabetes by whole exome sequencing and bioinformatic approaches. [PDF]
World J Diabetes, 2021 Sun SS, Wang RX.
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Clinical data and genetic mutation in Kallmann syndrome with CHARGE syndrome
, 2018 Jie Wen +4 more
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Fertility and fragrance: another cause of Kallmann syndrome [PDF]
, 2015 Шломо Мелмед
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