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Research 151–180 of 1000+
- Alopecia universalis after injection of messenger RNA COVID-19 vaccine. A case report
- Rehabilitation therapy for a severe case of coronavirus disease 2019: a case report
- Case 22
- Biotin Deficiency in an Infant Fed with Amino Acid Formula
- Trichoscopic Findings of Erosive Pustular Dermatosis of the Scalp Associated with Gefitinib
- Case Report. Kerion Celsi effectively treated with terbinafine. Characteristics of kerion Celsi in the elderly in Japan
- Ultrastructural characteristics of trichilemmal cysts: report of two cases
- Moth-Eaten Symptomatic Syphilitic Alopecia Associated with Human Immunodeficiency Virus—A Case Report
- Vogt-Koyanagi-Harada Disease in which Poliosis and Alopecia Occurred after a Long Period of Time.
- Changes in cuticle of scalp hair in mild acquired zinc deficiency: A study using scanning electron microscopy
- Stiffness of Human Hair Correlates with the Fractions of Cortical Cell Types
- Degree of Alignment Between Japanese Patients and Physicians on Alopecia Areata Disease Severity and Treatment Satisfaction: A Real-World Survey
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Decreased benzothiazole-type pheomelanin in regrown brown hair in alopecia areata
- Divergent progression pathways in male androgenetic alopecia and female pattern hair loss: Trichoscopic perspectives
- Hair transparency decoding in Asia: From stylists’ perception to in vitro measurement
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Combination Therapy to Treat Asian Female Pattern Hair Loss
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Multipotent nestin-expressing stem cells capable of forming neurons are located in the upper, middle and lower part of the vibrissa hair follicle
- Two-dimensional electrophoretic analysis of human hair keratins, especially hair matrix proteins
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Woolly hair generalizado: caso clínico e revisão da literatura
- Cryopreservation of engineered hair follicle germs for hair regenerative medicine
- ミレットエキス，パントテン酸カルシウム，L—シスチン，ビオチン含有食品の摂取による毛髪密度および頭髪の外観変化の検証試験
- Estrogen induce VEGF expression in dermal papilla cells