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Research 601–630 of 1000+
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Determination of finasteride and its metabolite in urine by dispersive liquid–liquid microextraction combined with field-enhanced sample stacking and sweeping
- RETRACTED: A two‐sample Mendelian randomization study of mutual relations of six types of diets in atopic dermatitis
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Epidermolysis Bullosa Simplex Keratinocytes Show Disturbed Mitochondrial Positioning and Activity
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Loose anagen hair syndrome in two patients with epidermolysis bullosa simplex, Dowling-Meara type
- Diffuse congenital hypotrichosis simplex with associated hair shaft fragility
- Sexual desire in a sample of married Egyptian women with polycystic ovarian syndrome
- Diffuse partial woolly hair in a patient with epidermolysis bullosa simplex with mottled pigmentation
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- 454 Modeling epidermolysis bullosa simplex with cardiomyopathy using KLHL24-mutant pluripotent stem cells.
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Isotretinoin-induced hair growth in a case of hereditary hypotrichosis simplex of the scalp: A promising therapeutic approach
- 603 Pathological modeling of epidermolysis bullosa simplex (EBS) using induced pluripotent stem cells (iPSC)
- Diagnosis by Hair Sample:A Rare Case of Netherton Syndrome in a 2-Year-Old Girl
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Successful treatment of hereditary hypotrichosis simplex by platelet rich plasma injection with topical minoxidil 2%
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Light microscopy of the hair: A simple tool to "untangle" hair disorders
- The genetic link between thyroid dysfunction and alopecia areata: a bidirectional two-sample Mendelian randomization study
- Enhancing germination performance and vigor of lettuce and napa cabbage seeds through simple seed priming techniques under controlled conditions
- Associations between genetically predicted sex and growth hormones and facial aging in the UK Biobank: a two−sample Mendelian randomization study
- Training Module in Hair Restoration Surgery: A Simple Method for Beginning Physicians and Assistants
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- Hair Root Dermoscopy from Shed Hair: A Simple Diagnostic Tool in Telogen Effluvium
- S236: Mandibular Trauma: From the Simple to the Complex and Everything in Between