36 citations
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July 2014 in “Neuromuscular Disorders” A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.
January 2025 in “Dermatology Reports” Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.
September 2000 in “Hair transplant forum international” The document's conclusion cannot be provided because the document is not accessible or understandable.
September 2023 in “Journal of The American Academy of Dermatology” Clinical trials for hair loss in the USA show differences in participation among different races and ethnic groups.
September 1998 in “Hair transplant forum international” The document's content could not be processed.
January 2025 in “Case Reports in Genetics” A rare gene variant causes sexual development issues in siblings, needing personalized treatment.
September 2025 in “Journal of the American Academy of Dermatology”
July 2016 in “Hair transplant forum international” The document's conclusion cannot be provided because the content is not available.
March 2009 in “European Urology Supplements” September 2023 in “Journal of the American Academy of Dermatology”
November 2018 in “Hair transplant forum international” The document's conclusion cannot be provided because the content is not accessible.
1 citations
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January 2003 in “Hair transplant forum international” The document's conclusion cannot be provided because the document is not accessible or understandable.
1 citations
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June 2022 in “Journal of Cosmetic Dermatology” Two specific genetic markers increase the risk of hair loss in Asian populations.
The document cannot be summarized as it is not provided or is unclear.
September 2017 in “Journal of Investigative Dermatology” RCS-01 is safe and may help rejuvenate aging skin.
2 citations
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July 1996 in “Hair transplant forum international” The document's conclusion cannot be provided because the document is not accessible or understandable.
September 2023 in “Zenodo (CERN European Organization for Nuclear Research)” The document's conclusion cannot be determined because the content is not available.
7 citations
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June 2011 in “Movement Disorders” A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.
January 2008 in “Hair transplant forum international” The document's conclusion cannot be provided as the content is not available.
June 2023 in “Zenodo (CERN European Organization for Nuclear Research)”
28 citations
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March 2010 in “British Journal of Dermatology” Genetic marker rs12558842 strongly linked to male hair loss.
53 citations
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May 1996 in “The Journal of Clinical Endocrinology & Metabolism” Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.
1 citations
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July 2025 in “Journal of Investigative Dermatology” 12 citations
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December 2013 in “Immunological Investigations” The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.
September 2017 in “Hair transplant forum international” The document's conclusion cannot be provided because the content is not available.
May 1999 in “Hair transplant forum international” The document cannot be processed or understood.
June 2018 in “International Review of Intellectual Property and Competition Law”
November 2015 in “Hair transplant forum international” The document's conclusion cannot be provided as the content is not available to parse.
12 citations
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June 2016 in “Clinical and experimental dermatology” A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.
4 citations
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January 2016 in “International journal of reproduction, contraception, obstetrics and gynecology” A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.