Search
for
Sort by
Research 181–210 of 1000+
- National scientific medical meeting 1996 abstracts
- Progeroide Syndrome
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- “Structural imprinting” of the cutaneous immune effector function
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Transglutaminase Activity Is Conserved in Stratified Epithelia and Skin Appendages of Mammals and Birds
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- E-Poster
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Alopecia frontal fibrosante: revisão bibliográfica dos aspectos gerais, fisiopatológicos, diagnósticos e do tratamento
- Ichthyosis Follicularis with Alopecia and Photophobia Syndrome (IFAP): A Case Report and Review of the Literature
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Distancia promedio de la línea de implantación pilosa frontal y sus estructuras en una población de mujeres colombianas
- ALOPECIA AREATA-A CLINICAL ANALYSIS
- Nonscarring hair loss disorders
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Treatment of alopecia totalis/universalis/focalis with vitamin D and analogs: Three case reports and a literature review
- Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areata
- Central nervous system involvement in autoimmune polyglandular syndrome
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- A Review on Ayurvedic Niadanatmak Concept of Khalityavyadhi
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy