Search
for
Sort by
Research 571–600 of 1000+
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- Monilethrix in three generations
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Genomic Analysis of Trichotillomania
- Supplementary Material for: Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping
- Supplementary Material for: Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping
- The Review On "Alopecia Areata: A Compressive Review of Pathogenesis, Diagnosis, Clinical Pattern and Remedies
- From Hair-Pulling to Trichobezoars and Rapunzel Syndrome: A Comprehensive Review of Trichotillomania
- Uncombable hair in a case of Zellweger syndrome – A new association
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Mind the hair
- 017 Lichen Planus Colocalized with Vitiligo: Coincidence?
- Cicatricial alopecia: What’s new in etiology?
- Monilethrix: the use of tricoscopy in clinical diagnosis
- Bamboo Hair Syndrome or Netherton Syndrome - A Case Report
- Androgens in women
- Skin diseases associated with atopic dermatitis
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Hidradenitis Suppurativa: From Physiopathologies to Targeted Therapeutics
- Hidradenitis Suppurativa: From Physiopathologies to Targeted Therapeutics
- TRANSTORNOS DISSOCIATIVOS EM PACIENTES VÍTIMAS DE ABUSO SEXUAL NA INFÂNCIA
- Generation of a Novel Inducible and Dermal Papilla‐Specific <i>Wif1‐CreER</i> Knock‐In Mouse Line for Hair Follicle Research
- A BRIEF STUDY ON ALOPECIA AREATA
- [An infant with short stature and red cheeks (Rothmund-Thomson syndrome)].
- A clinical case of CNOT3 syndrome in a 10-year-old girl
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Congenital Adrenal Hyperplasia
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies