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Research 961–990 of 1000+
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- Genetic analysis does not confirm non-classical congenital adrenal hyperplasia in more than a third of the women followed with this diagnosis
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- GLOMERULAR MEMBRANOUS NEPHROPATHY AND WERNER SYNDROME: A CASE REPORT
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Netherton Syndrome – Responding to Oral Retinoids
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- 155 Exploring perceived quality of life in middle- to old-aged patients with inherited ichthyosis: a qualitative study
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Treatment of erythromelanosis follicularis faciei et colli with a 595‐nm pulsed dye laser
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Efficacy of Dupilumab in Treating Atopic Dermatitis With Recurrent Eczema Herpeticum in a Patient With DOCK8-Deficiency Hyper-IgE Syndrome: A Case Report
- Uncombable hair improved by biotin
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- A Rare Case of Severe Acrodermatitis Enteropathica During Covid-19 Lockdown.
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Congenital Adrenal Hyperplasia
- Disorders of Hair Pigmentation
- A case of acrodermatitis enteropathica misdiagnosed as staphylococcal scalded skin syndrome
- Dermatologic Disorders
- A polarizing light microscopy can be an easy and reliable diagnostic tool of congenital keratinizing disorders including Netherton syndrome
- Ichthyoses
- Female Androgenetic (?) Alopecia
- Nanostructured Drug Delivery Systems for Targeting 5-α-Reductase Inhibitors to the Hair Follicle
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield