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Research 151–180 of 227
- Disorders of Keratinization
- KERATINS AND SKIN DISORDERS
- The keratins and their disorders
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- A General Paediatric Approach to Ankyloblepharon–Ectodermal Dysplasia–Cleft Lip/Palate Syndrome in Infancy: A Case Report
- Netherton Syndrome Associated with Growth Hormone Deficiency
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Manifest hair repigmentation associated with etretinate therapy
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Surgical approach of ectropion in lamellar ichthyosis
- Ischemic onycholysis of the hands
- Dupilumab in a 9-week-old with Netherton Syndrome Leads to Deep Symptom Control
- Disorders of hair in children
- Atypical Juvenile Pityriasis Rubra Pilaris: A Case Report of Early Onset With Late Diagnosis
- The human keratins: biology and pathology
- Keratin disorders: from gene to therapy
- Congenital hair loss disorders: Rare, but not too rare
- Síndrome do nevo de Becker
- Congenital atrichia and hypotrichosis
- Molecular Genetics of Alopecias
- Both low circulating insulin-like growth factor-1 and high-density lipoprotein cholesterol are associated with hair loss in middle-aged women
- Chemotherapy and the Skin: Understanding Dermatologic Side Effects
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Collodion baby case series: the success of oral retinoic acid
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- 152 Alopecia patterns in patients with autosomal receesive congenital ichthyosis
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Trichothiodystrophy in a child with occult learning disorder
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities