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Research 511–540 of 1000+
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- Hair as an Index of Protein Malnutrition
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- Chronic nonhealing ulcer in a finger of a toddler – a rare presentation of the hair thread tourniquet syndrome
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation
- Nonclassical Congenital Adrenal Hyperplasia and Pregnancy
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- Prepubertal Fibrosing Alopecia in a Pattern Distribution
- Linear Alopecia Areata in a 4-year-old Patient: A Rare Clinical Variant
- PO-0172 Behind Closed Doors: The Effects Of Childhood Cancer On Somatic Health Of Parents During And After Oncologic Therapy
- Розробка лінійки косметичних засобів по догляду за волоссям з екстрактом перцю чилі
- The Myth of Beneficent Nature: The Risks of Herbal Preparations
- The structure of people’s hair
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- Hair Loss in Children
- Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
- Childhood Alopecia: Patent and Treatment Method
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Alopecia Areata in Children: Quality of Life for Children and Their Parents
- Combination of light-emitting diode with minoxidil 2%, topical corticosteroid and oral immunomodulator induced hair regrowth in a pediatric alopecia areata
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Dermoscopic evaluation of tinea capitis: A case report
- Uncombable hair syndrome: A case presentation
- Metabolic disease with autoimmune phenomena: 2 cases of SLE-like disease in young children diagnosed with lysinuric protein intolerance
- CROSS-META-ANALYSIS ON POLICOSANOL BIOREFINING: AN INNOVATIVE TECHNOLOGY PROSPECTING PROTOCOL WITH IBERO-AMERICAN INSIGHTS
- Highlights
- Trichotillomania in children and adolescents: Review of the literature and case report
- Neurotrichosis: Hair‐shaft Abnormalities associated with Neurological Diseases
- Trichilemmal cyst of the eyelid: An unusual presentation in paediatric age group