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- Sparse hairs below frontal hair line are early sign of androgenetic alopecia in men
- Sparse Hair on the Scalp
- Loss of epidermal PLCg1 induced sebaceous gland hyperplasia and sparse hair
- Sparse hair in a female toddler
- Sparse Brittle Hair and Bilateral Temporal Alopecia in a Child
- Coupled 3D reconstruction of sparse facial hair and skin
- Normalization of hair growth in sparse fur-abnormal skin and hair (SPF-ASH) mice by introduction of the rat ornithine transcarbamylase (OTC) gene
- Bead-jet printing enabled sparse mesenchymal stem cell patterning augments skeletal muscle and hair follicle regeneration
- Faculty Opinions recommendation of Bead-jet printing enabled sparse mesenchymal stem cell patterning augments skeletal muscle and hair follicle regeneration.
- 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
- Evaluation of hair structural abnormalities in children with different neurological diseases
- Nail and hair changes in chronic kidney disease patients
- 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
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Two females with hair loss
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hair: more than just an appendage
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- PEDL-XAI: A Hybrid Probabilistic Ensemble Deep Learning Approach for Hair Disorder Diagnosis
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Anhidrotic Ectodermal Dysplasia: Predisposition to Bronchial Disease
- Ectodysplasin research—Where to next?
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Histopathology of Hypotrichosis with Juvenile Macular Dystrophy
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Diagnosis of Trichothiodystrophy in 2 Siblings
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response