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research Hair diseases
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research References
research References
research References
research Laser-Guided Hairline Design and Donor Strip Marking
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research A Word from Helen
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research 22
research Integrated Business Intelligent System for E-Health: A Case for Dermatology Diseases
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research P5 Assembly of hair keratins in thansfected cultured cells
research Diffuse congenital hypotrichosis simplex with associated hair shaft fragility
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research Part 2: LLLT Devices, Medical Device Regulation, and Impact on Development
Strict regulations may slow down new LLLT treatments.
research Letters to the Editors
research Improved trichoscopic assessment of yellow dots using Sub-Ultraviolet Light
research Improved trichoscopic assessment of yellow dots using Sub-Ultraviolet Light
research Contents Vol. 207, 2003
research Volume Contents
research Volume Contents
research Hypertrichosis lanuginosa acquisita following cytotoxic chemotherapy
Some cancer treatments can cause abnormal fine hair growth.
research MAGİSTRAL AVTOMOBİL YOLLARI. TARIXİ, TORPAQ SAHƏSİ, MÜASİR VƏZİYYƏTİ, PROBLEMLƏRİ
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research Telogen Effluvium: Tips
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research Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.
research EXPRESSION OF HLA-DR IN HAIR FOLLICLES IN ALOPECIA AREATA
research Harlequin Ichthyosis
research Hair-Thread Tourniquet Syndrome; Emergent Diagnosable Condition
Hair-Thread Tourniquet Syndrome is a rare condition where hair or thread tightly wraps around a child's body part, requiring quick treatment to prevent damage.
research Screening of Helicobacter pylori Infection in patients with Telogen Effluvium (Original article)
H. pylori infection may be linked to the hair shedding condition Telogen Effluvium.
research Advertiser Beware
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research Overexpression of cotton Trihelix transcription factor GhGT-3b_A04 enhances resistance to Verticillium dahliae and affects plant growth in Arabidopsis thaliana
research Homozygous missense mutation in theLIPHgene causing autosomal recessive hypotrichosis simplex in a Chinese patient
A specific gene mutation causes a rare hair loss condition in a Chinese patient.
research WAHRS Live Surgery Workshop Highlights
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