November 1998 in “Hair transplant forum international” The document's conclusion cannot be provided because the content is not accessible.
5 citations
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March 2005 in “Journal of The American Academy of Dermatology”
January 2017 in “Hair transplant forum international” The document's content could not be processed.
July 2010 in “Hair transplant forum international” The document cannot be processed to provide a conclusion.
1 citations
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January 2018 in “Medical Science and Discovery” The document's conclusion cannot be provided as the content is not available for parsing.
June 1996 in “Journal of Dermatological Science”
72 citations
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November 2012 in “PloS one” The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.
11 citations
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October 2001 in “Dermatologic Clinics” The document concludes that DAB389-IL2 is promising for treating refractory cutaneous T-cell lymphoma, but more research is needed on its effectiveness and side effect management.
November 2018 in “Hair transplant forum international” The document's content couldn't be processed for a summary.
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.
15 citations
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January 2010 in “Reproduction, Fertility and Development” A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.
November 2014 in “International Society of Hair Restoration Surgery”
November 1995 in “Hair transplant forum international” The document cannot be understood or processed.
75 citations
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September 2016 in “EMBO journal” PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.
June 2014 in “The Journal of Dermatology” A patient with a rare chromosome condition also had a rare type of hair loss.
September 2023 in “Journal of The American Academy of Dermatology” Patients with skin cancer on the scalp and ear in Mexico have specific features and results from their treatments.
November 2000 in “Hair transplant forum international” The document's conclusion cannot be provided because the content is not accessible.
CG2001 is safe, well-tolerated, and a promising treatment for hair loss with fewer side effects.
July 2025 in “Journal of Investigative Dermatology”
6 citations
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February 2004 in “Clinical and Experimental Ophthalmology” The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.
1 citations
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September 2020 in “Journal of dermatology” Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.
21 citations
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March 2015 in “Neurological Sciences” A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.
November 2016 in “Hair transplant forum international” The document's content couldn't be processed to provide a conclusion.
April 2016 in “The Journal of Sexual Medicine”
August 2025 in “Advanced Science” The corrections confirm the original findings on scarless hair follicle regeneration.
3 citations
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June 2022 in “European journal of human genetics” A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.
November 2016 in “Hair transplant forum international” Apologies, but I can't provide the information you're looking for.
1 citations
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February 2012