• A case report of Lhermitte-Duclos disease with systematic AVMs
• Arteriovenous and lymphatic malformations, linear verrucous epidermal nevus and mild overgrowth: another hamartoneoplastic syndrome?
• Assessing Cutaneous Mosaicism at the Molecular Level
• Autopsy case of linear nevus sebaceous syndrome with KRAS (G12D) mutation
• Basal-cell and linear unilateral adnexal hamartoma (or linear unilateral basal-cell nevus)
• Basaloid Follicular Hamartoma: A Case Report and a Novel Cosmetic Treatment
• Chromosomal mosaicism in two patients with epidermal verrucous nevus. Demonstration of chromosomal breakpoint
• Clinical differentiation between Proteus syndrome and hemihyperplasia: description of a distinct form of hemihyperplasia
• Coexistence of two neurocutaneous syndromes: tuberous sclerosis and hypomelanosis of Ito
• Congenital linear unilateral basal cell nevus: a case report with patched gene molecular studies
• Congenital lipomatous tumour, presented as a polypoidal projection on upper eyelid
• Craniofacial hyperostoses in Proteus syndrome -- a case report
• Cutaneous inflammation as a marker of malignant transformation in a patient with linear unilateral basaloid follicular hamartoma
• Dynamics and structural stability effects of germline PTEN mutations associated with cancer versus autism phenotypes
• Epidermal nevi
• Epidermal nevus syndrome
• Epidermal nevus syndrome
• Epidermal verrucous linear inflammatory hamartoma (3 cases)
• Epilepsy associated with tuberous sclerosis complex in childhood: Long-term outcome in children after epilepsy surgery and children non-eligible for epilepsy surgery
• Exploring an objective measure of overactivity in children with rare genetic syndromes
• First Reported Case of 'Epidermal Nevus Syndrome' with a Triad of Central Nervous System Deformities
• Genetic aspects of neurocutaneous disorders
• Hamartomas
• Happle-Tinschert syndrome variable phenotype as part of the mosaic hedgehog spectrum: Report of three cases
• Happle-Tinschert syndrome. Segmentally arranged basaloid follicular hamartomas, linear atrophoderma with hypo- and hyperpigmentation, enamel defects, ipsilateral hypertrichosis, and skeletal and cerebral anomalies
• Happle-Tinschert, Curry-Jones and segmental basal cell naevus syndromes, overlapping disorders caused by somatic mutations in hedgehog signalling genes: the mosaic hedgehog spectrum
• Hemimegalencephaly and linear nevus sebaceous syndrome
• Histopathological study of basaloid follicular hamartoma
• Increased expression of L-amino acid transporters in balloon cells of tuberous sclerosis
• Inner ear malformations and hearing loss in linear nevus sebaceous syndrome
• Lhermitte-Duclos disease associated with dysembryoplastic neuroepithelial tumor differentiation with characteristic magnetic resonance appearance of "tiger striping"
• Linear Cowden nevus: a new distinct epidermal nevus
• Linear epidermal nevus and nevus sebaceus syndromes: a clinicopathologic study of 3 patients
• Linear intraoral lesions in the sebaceous nevus syndrome
• Linear naevus sebaceous syndrome, optic disc staphyloma, and non-rhegmatogenous retinal detachment
• Linear nevi, hemihypertrophy, connective tissue hamartomas, and unusual neoplasms in children
• Linear nevus sebaceous syndrome
• Linear sebaceous nevus syndrome
• Linear sebaceous nevus syndrome (sebaceous nevus of Jadassohn) associated with abnormal neuronal migration and optic glioma: case report
• Linear sebaceous nevus syndrome. A hamartoma variant
• Linear trichilemmomas on the ankle of a 28-year-old female
• Linear unilateral basal cell nevus: a benign follicular hamartoma simulating multiple basal cell carcinomas
• LKB1 tumor suppressor protein regulates actin filament assembly through Rho and its exchange factor Dbl independently of kinase activity
• Longitudinal neurobehavioral profiles in children and young adults with PTEN hamartoma tumor syndrome and reliable methods for assessing neurobehavioral change
• More association of linear sebaceous nevus syndrome and unilateral megalencephaly
• Multiple basaloid follicular hamartomas associated with acrochordons, seborrhoeic keratoses and chondrosarcoma
• Multiple cutaneous linear neuromas
• Multiple hamartomas associated with intracranial malformation
• Neurologic manifestations of the organoid nevus syndrome
• Nevus Comedonicus Syndrome Associated with Psychiatric Disorder
• New syndrome: focal dermal hypoplasia, morning glory anomaly, and polymicrogyria
• Ophthalmic manifestations of linear nevus sebaceous/organoid nevus syndrome
• Organoid nevus syndrome (linear nevus sebaceus of Jadassohn): clinical and radiological study of a case
• Pathogenetic insights from quantification of the cerebriform connective tissue nevus in Proteus syndrome
• Pathology of osseous and genitourinary lesions of Proteus syndrome
• Perioperative management of infants with the linear naevus sebaceous syndrome of Jadassohn: a report of two cases
• Pigmented linear plaque on the upper limb
• Proteus syndrome
• Proteus syndrome: an expanded phenotype
• Proteus syndrome: clinical evidence for somatic mosaicism and selective review
• Proton magnetic resonance spectroscopy of linear nevus sebaceus syndrome
• Recurrent Lhermitte-Duclos disease: report of two cases and association with Cowden's disease
• Schimmelpenning-Feuerstein-Mims syndrome (SFM syndrome)
• Schimmelpenning-Feuerstein-Mims syndrome and its neurologic manifestations. 6 personal cases and review of the literature
• Sebaceous nevus of Jadassohn: review and clinical-surgical approach
• Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity
• Skeletal involvement and follow-up in linear nevus sebaceous syndrome
• Sleep Problems in Children With Neurocutaneous Syndromes: A Cross-Sectional Study
• Solomon's epidermal nevus syndrome (type: linear nevus sebaceus) and hypophosphatemic vitamin D-resistant rickets
• The Bannayan syndrome: an autosomal dominant disorder consisting of macrocephaly, lipomas, hemangiomas, and risk for intracranial tumors
• The CHILD nevus: a distinct skin disorder
• The sebaceous nevus as part of the Schimmelpenning-Feuerstein-Mims Syndrome--an obvious phacomatosis first documented in 1927
• Tuberous sclerosis complex: the role of patient's history and clinical examination
• Unilateral focal dermal hypoplasia
• Unilateral linear basal cell nevus associated with diffuse osteoma cutis, unilateral anodontia, and abnormal bone mineralization
• Unilateral linear basaloid follicular hamartoma: Its diagnosis and successful treatment with surgical excision and adjuvant dermabrasion
• Unilateral megalencephaly in linear nevus sebaceous syndrome: a neuroradiological case report
• Verrucous epidermal nevus as a manifestation of a type 2 mosaic PTEN mutation in Cowden syndrome
• Visceral adiposity in patients with lipomatous hypertrophy of the interatrial septum
• Whorled hairless nevus of the scalp, linear hyperpigmentation, and telangiectatic nevi of the lower limbs: a novel variant of the "phacomatosis complex"