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- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Bachmann–Bupp syndrome and treatment
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- A guide to diagnosis and management of hypertrichosis
- [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?].
- Bilateral Xen is Used as Minimally Invasive Glaucoma Surgery for Glaucoma in GAPO Syndrome: Case Report
- Male fertility and skin diseases
- Clinical Experience With Tissue Expansion
- Oral Manifestations of Hematologic and Nutritional Diseases
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Low level of maternal biotin intake changes the expression of biotin transporter in dams and fetuses in mice
- Use of chemotherapy during human pregnancy
- Pharmacologic Modulation of Sebaceous Gland Activity: Mechanisms and Clinical Applications
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- The clinical spectrum of parathyroid disease
- Gonads
- Syndromes of Severe Insulin Resistance (SSIRs)
- Progeroide Syndrome
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Avian-Inspired Analogies in Dermatology
- Safety of Common Medications for Treating Dermatology Disorders in Pregnant Women
- TONGUE, RED
- Toxic and Metabolic Disorders of the Nervous System
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma