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Research 301–330 of 1000+
- Gestational Thyroid Dysfunction in a Sub-District Area of Pampore, Kashmir: A Cross-Sectional Study
- Research Trend of Studies Regarding the Change and Treatment of the Skin on Pregnant Women in the Last Decade: A Systematic Review and Bibliometric Analysis
- Tourniquet syndrome in children (literature review and own observation)
- Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome
- Psychosocial Aspects of Skin Conditions and Diseases
- The First Report of Isolated Clitoral Hood Hair-Thread Tourniquet Syndrome: A Study of Six Patients
- Correction of Diffuse Alopecia in Iron Deficiency Anemia
- Restolin Hair Supplement: Here are Some Effective Remedies for Hair Fall Control! v1
- Interrelationships between Skin Structure, Function, and Microbiome of Pregnant Females and Their Newborns: Study Protocol for a Prospective Cohort Study
- Hallmark evidence of lipopolysaccharide (LPS) tolerance in obese women with polycystic ovary syndrome (PCOS) - LPS-induced NFkB suppression in mononuclear cells (MNC) is linked to hyperandrogenism in PCOS
- 675 Hair loss in hephaestin knockout mice is associated with iron deficiency
- Hair Tourniquet Syndrome, A missed diagnosis: Review of Literature
- Appropriate use of metformin in early pregnancy: is there a role for first trimester use?
- Hair shedding in women
- Generation of an intestinal‐specific hephaestin knockout mouse
- Incidence and risk factors for neonatal occipital alopecia: A retrospective study
- The clinical features and long time follow-up of neonatal lupus erythematosus in 12 children
- Parents May Over-report Use of Home Safety Interventions
- Rates of polycystic ovary syndrome (PCOS) symptoms in relatives of patients with PCOS
- Iatrogen male infertility
- Prenatal serological diagnosis of intrauterine cytomegalovirus infection.
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- Trichotillomania in children and adolescents: Review of the literature and case report
- Hypertrichosis cubiti (hairy elbows) and short stature: a recognisable association.
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Crystalline Cataract and Uncombable Hair
- Physiologic changes and dermatoses of pregnancy
- Successful Treatment of Temporal Triangular Alopecia with Topical Minoxidil