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Research 691–720 of 1000+
- Characterization of<i>CDH3</i>-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Histopathology of Hypotrichosis with Juvenile Macular Dystrophy
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
- Cutaneuos findings in patients with predialysis chronic kidney disease
- Diagnosis of Trichothiodystrophy in 2 Siblings
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Werewolf, there wolf: variants in <i>Hairless</i> associated with hypotrichia and roaning in the lykoi cat breed
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- A study on common clinical pattern of presentation of skin and hair changes in nutritional deficiencies associated with dietary fallacies in children 1 to 5 years of age
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- A forgotten and hidden disease
- Redução da região frontal com incisão pré-capilar: relato de experiência e indicações
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- PEDL-XAI: A Hybrid Probabilistic Ensemble Deep Learning Approach for Hair Disorder Diagnosis
- Widespread erythematous scaly eruption in an infant with phenylketonuria
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Multiple facial atrophic scars in childhood
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Evaluation of hair structural abnormalities in children with different neurological diseases
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- A Rare Case of Severe Acrodermatitis Enteropathica During Covid-19 Lockdown.
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Hair: more than just an appendage
- Nail and hair changes in chronic kidney disease patients
- A 9-month-old infant with severe scalp dermatosis
- The eyelash comes to the fore