Search
for
Sort by
Research 601–630 of 1000+
- Sparse hairs below frontal hair line are early sign of androgenetic alopecia in men
- Sparse Brittle Hair and Bilateral Temporal Alopecia in a Child
- Sparse haplotype-based fine-scale local ancestry inference at scale reveals recent selection on immune responses
- Sparse Hair on the Scalp
- Loss of epidermal PLCg1 induced sebaceous gland hyperplasia and sparse hair
- 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.
- Keratinocytes and Adipose-derived mesenchymal stem cells : The heir and the spare to regenerative cellular therapies for difficult-to-heal skin wounds
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- 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
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Anhidrotic Ectodermal Dysplasia: Predisposition to Bronchial Disease
- Ectodysplasin research—Where to next?
- 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
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- Werewolf, there wolf: variants in <i>Hairless</i> associated with hypotrichia and roaning in the lykoi cat breed
- 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
- 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
- Multiple facial atrophic scars in childhood