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- Ptosis in childhood
- Congenital ptosis repair with a frontalis silicon sling: comparison between Fox's single pentagon technique and a modified Crawford double triangle technique
- Congenital ptosis: Long-term outcome of frontalis suspension using autogenous temporal fascia or fascia lata in children
- Bilateral nevus comedonicus of the eyelids: An unusual cause of ptosis and ectropion
- Obesity and the skin
- Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications
- Cosmetic surgery in men
- PRESEPTAL CELLULITIS DUE TO IMPETIGO – A CASE REPORT OF UNCOMMON PRESENTATION IN PAKISTAN
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Dermatologic manifestations of endocrine disorders
- Stress-related skin disorders
- How to diagnose a lipodystrophy syndrome
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Male fertility and skin diseases
- The eye and the skin in endocrine metabolic diseases
- Diseases of Periocular Hair
- Current and future pharmacotherapy for alopecia areata
- Geriatric Dermatologic Therapy
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Part Three (Cure Most Diseases by Logical Nutrition Treatment): The Society Agent Simulating (SAS) & Usage of Oral and Dental Diseases to Predict Criminals Earlier
- Genetic Defects of Female Sexual Differentiation
- Gonads
- National scientific medical meeting 1996 abstracts
- Interrelation of immunity and tissue repair or regeneration
- Refractory Myasthenia Gravis and Concurrent Alopecia Areata Postthymectomy With Improvements After Cortisone Taper: A Case Report
- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia