research Message from the ISHRS 2016 World Congress Program Chair
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research Fine mapping of the human AR/EDA2R locus in androgenetic alopecia
Genetic marker rs12558842 strongly linked to male hair loss.
research Female pattern hair loss
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research Finasteride fra luci ed ombre
research Suspected cases of pulmonary tuberculosis referred from port of entry.
research Dermatology for the Non-Dermatologist: Triangular Alopecia
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research 0749 Serine and arginine-rich splicing factor 3 regulates epidermal differentiation in cutaneous squamous cell carcinoma
research Salute to Surgeon of the Month
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research A Proposal from Steven C. Chang, MD
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research Report on the 6th Congress and Live Surgery Workshop of the ESHRS Berlin, GermanyFriday, May 30, 2003Saturday, May 31, 2003Sunday, June 1, 2003
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research Bosley Hair Restoration in Miami _110
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research Letter: Repair of severed brachial plexus.
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research Birt-Hogg-Dube Syndrome with a Novel Mutation in the FLCN Gene
A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.
research Hair Symposium 1996 — The New York Experience
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research Pearls of Wisdom
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research Surgical Assistants Editor’s Message
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research Pioneer of the Month: William R. Rassman, MD
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research Androgenetic Alopecia-Reply
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research 198 Dutasteride for men with androgenic alopecia unresponsive to finasteride
research Identification and Expression of the Target Gene SLC24A2 of oar-miR-377 and Its Novel SNPs Effects on Wool Traits in Sheep
A specific genetic variation affects wool quality in sheep.
research Message from the ISHRS 2018 World Congress Program Chair
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research Message from the ISHRS 2018 World Congress Program Chair
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research Message from the ISHRS 2018 World Congress Program Chair
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research Message from the ISHRS 2018 World Congress Program Chair
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research P0401 Finasteride 1 mg: Silent impacts on male fertility despite preserved hormonal balance
research 112 Post-Finasteride Syndrome – Outcomes of FDA Database
research WAHRS Live Surgery Workshop Highlights
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research Message from the ISHRS 2016 World Congress: Program Chair
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research C2orf37 mutational spectrum in Woodhouse–Sakati syndrome patients
Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.
research Male androgenetic alopecia
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