Search
for
Sort by
Research 421–450 of 1000+
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Low‐dose oral minoxidil in alopecia: evaluating blood pressure changes in patients with abnormal blood pressure—a retrospective study
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Role of Dermal Factors Involved in Regulating the Melanin and Melanogenesis of Mammalian Melanocytes in Normal and Abnormal Skin
- Corkscrew Hair: A New Dermoscopic Sign for Diagnosis of Tinea Capitis in Black Children
- Extracellular Vesicles in Skin Wound Healing
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- Trichodysplasia spinulosa associated with chemotherapy for acute lymphocytic leukaemia
- The ophthalmological complications of targeted agents in cancer therapy: what do we need to know as ophthalmologists?
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Familial and Sporadic Porphyria Cutanea Tarda
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat
- The character “hairless” in the mouse
- Cholesterol homeostasis: Links to hair follicle biology and hair disorders
- Dermatotoxicology of microneedles (MNs) in man
- White monkey syndrome in infant baboons (Papio species)
- Dermabrasion
- Séquelles cutanéomuqueuses et oculaires des SJS et de Lyell
- Cetuximab-induced hypertrichosis of the scalp and eyelashes
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- <i>In vivo</i> and <i>in silico</i> evaluation of the ameliorative effect of hesperidin on finasteride-induced testicular oxidative stress in Wistar rats
- [An infant with short stature and red cheeks (Rothmund-Thomson syndrome)].
- Evaluation of dermatologic adverse events associated with aromatase inhibitors: insights from the FAERS database
- The Association between Metabolic Syndrome Components and Hair Loss both Male and Female Individuals
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- ANTI-MÜLLERIAN HORMONE LEVEL AS A PREDICTIVE FACTOR IN THE DIAGNOSIS OF POLYCYSTIC OVARIAN SYNDROME IN DUHOK PROVINCE – KURDISTAN REGION, IRAQ