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540-570 / 1000+ results research Cyberspace Chat
research Cyberspace Chat
research Message from the 2017 Surgical Assistants Vice Chair
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research 0955 Selective BET inhibition as potential hidradenitis suppurativa treatment
research Surgeon of the month
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research Surgical Assistant’s Pearl on Graft Cutting
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research Letters to the Editors: Re: Use of unlicensed practitioners
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research 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.
research Citalopram and finasteride with the lot number FI0510058-A have been voluntarily recalled by Greenstone, after a labelling error
research Tissue Dynamics in the Three-Hair-Bearing Flap Transposition
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research Devices and genomic therapies
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research My Clinical Experience with Needle and Laser SMP Devices
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research Novel de novo pathogenic variant in the ODC1 gene in a girl with developmental delay, alopecia, and dysmorphic features
A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.
research 10.1063/5.0132123.1
research ABHRS news
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research Innovative Device for Indocianyne Green Navigational Surgery
The new device improves surgical accuracy by using a special dye and camera to see inside tissues.
research LIGA R and D and prototyping[Lithography, Electroforming, and Assembly]
research Society and Forum Separate Financially
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research First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.
research Salute to Jung-Chul Kim, MD, PhD: Surgeon of the Month
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research Ablative 2940 nm Er: YAG fractional laser for male androgenetic alopecia
research Controversies: Where Business Meets Medicine
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research Letters to the Editors: Re: FUE and donor planning
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research 200 Uncommon finasteride side effects in male androgenic alopecia
research Miscellaneous Exosome Trials
research Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
research 842Combination therapy with rofecoxib and finasteride in the treatment of men with lower urinary tract symptoms (LUTS)
research Association of single nucleotide polymorphisms in the RAB5B gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.
research The Free Communications of the Eighth Clinical Congress (Virtual) of the Gulf Chapter of the American Association of Clinical Endocrinologists; November 5–7, 2020
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