• [Translated article] Bilateral Temporal Arachnoid Cysts Associated With Phakomatosis Cesioflammea
• <em>Cutis tricolor</em>: a literature review and report of five new cases
• <em>GNA11</em> brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis
• A Case of Phacomatosis Pigmentovascularis Type IIa in a Korean Infant
• A case of phakomatosis pigmentovascularis type II: port-wine stain and dermal melanocytosis with cutis marmorata telangiectatica congenita-like lesions
• A female infant with phacomatosis pigmentovascularis and congenital chylous ascites: A case report
• A Neonatal Case of Phacomatosis Pigmentovascularis Type IIa
• A rare case of phakomatosis pigmentovascularis type IIb associated with inverse Klippel-Trenaunay syndrome and Sturge-Weber syndrome
• An unusual case of phakomatosis pigmentovascularis type IIb with Becker's nevus
• Bilateral Phacomatosis Pigmentovascularis in a Young Male with Developmental Glaucoma and Varicose Veins
• Bilateral Temporal Arachnoid Cysts Associated With Phakomatosis Cesioflammea
• Blotchy baby: a case of phakomatosis pigmentovascularis
• Born in the Purple: An Exceptional Case of Cutis Marmorata Telangiectatica Congenita
• Choroidal melanoma in phacomatosis pigmentovascularis cesioflammea
• Choroidal melanoma in phacomatosis pigmentovascularis cesioflammea
• CHOROIDAL MELANOMA IN PHAKOMATOSIS PIGMENTOVASCULARIS WITH KLIPPEL-TRENAUNAY SYNDROME
• CHOROIDAL MELANOMA IN PHAKOMATOSIS PIGMENTOVASCULARIS WITH OVERLAPPING STURGE-WEBER SYNDROME AND KLIPPEL-TRENAUNAY SYNDROME
• Clinical characteristics and treatment of 52 cases of phakomatosis pigmentovascularis
• Complete agenesis of the corpus callosum in phacomatosis pigmentovascularis cesioflammea: a manifestation of mosaicism?
• Congenital telangiectatic und pigmented lesions associated with lymphedema, difference in leg length, and scoliosis
• Cutis marmorata telangiectatica congenita and aberrant Mongolian spots: Type V phacomatosis pigmentovascularis or phacomatosis cesiomarmorata
• Dermoscopic features of Phakomatosis pigmentovascularis type II: An underutilized tool!
• Early-Onset Glaucoma Manifesting as Buphthalmos in an Infant with Phakomatosis Pigmentovascularis Type IIa
• Extensive red and blue patches in a young girl
• Extensive subarachnoid venous angiomatosis with hydrocephalus in phacomatosis pigmentovascularis
• Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review
• Fluorescein angiography findings in phacomatosis pigmentovascularis
• Glaucoma in Phacomatosis Pigmentovascularis in a Young African Adolescent Boy: A Case Report
• GNA11 brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis
• Hematoporphyrin monomethyl ether-mediated photodynamic therapy for phakomatosis pigmentovascularis type Ⅱ: A case report
• Hematoporphyrin monomethyl ether-mediated photodynamic therapy temporarily relieves severe pruritis from phakomatosis pigmentovascularis: A case report
• Intramedullary and retroperitoneal melanocytic tumor associated with congenital blue nevus and nevus flammeus: an uncommon combination of neurocutaneous melanosis and phacomatosis pigmentovascularis--case report
• Introduction to phacomatoses (neurocutaneous disorders) in childhood
• Kikuchi-Fujimoto disease in patient with systemic phacomatosis pigmentovascularis
• Laser therapy treatment of phacomatosis pigmentovascularis type II: two case reports
• Mongolian spots combined with halo-like disappearance surrounding café au lait spots
• Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis
• Mosaic GNA11 mutations and a second hit in KRAS in phakomatosis pigmentovascularis are associated with intraosseous arteriovenous malformations in the jaw
• Mosaic Neurocutaneous Disorders and Their Causes
• Mosaic neurofibromatosis type 1, not phacomatosis pigmentovascularis
• Naevus vascularis mixtus and mixed vascular naevus syndrome
• New case of phacomatosis cesio-flammeo-marmorata: the time is right to review the classification for phacomatosis pigmentovascularis
• Ocular features in a patient presenting with a rare combination of multiple phakomatoses
• Ocular manifestations in phakomatosis pigmentovascularis: Current concepts on pathogenesis, diagnosis, and management
• Ocular manifestations of facial port-wine stain, nevus of Ota, and phakomatosis pigmentovascularis in Asian patients
• Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions?
• Oral healthcare management of a child with phakomatosis pigmentovascularis associated with bilateral Sturge-Weber syndrome
• Outcomes of Infantile-Onset Glaucoma Associated With Port Wine Birthmarks and Other Periocular Cutaneous Vascular Malformation
• Outcomes of Management of Glaucoma in Phacomatosis Pigmentovascularis Over the Last Three Decades: A Single-Center Experience
• Outcomes of Microcatheter-Assisted Trabeculotomy for Glaucoma Associated With Sturge-Weber Syndrome and Phakomatosis Pigmentovascularis
• Pathophysiology and management of glaucoma associated with phakomatoses
• Patient with extensive Mongolian spots, nevus flammeus and nevus vascularis mixtus: A novel case of phacomatosis pigmentovascularis
• Phacomatosis cesioflammea in association with von Recklinghausen disease (neurofibromatosis type I)
• Phacomatosis Cesioflammea with Cutis Marmorata-like Lesions and Unusual Extracutaneous Abnormalities: Is It a Distinct disorder?
• Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association
• Phacomatosis cesiomarmorata with hypospadias and phacomatosis cesioflammea with Sturge-Weber syndrome, Klippel-Trenaunay syndrome and aplasia of veins -- case reports with rare associations
• Phacomatosis is Not a Twin-Spot Phenomenon
• Phacomatosis melanocesioflammea: the rediscovery of phacomatosis pigmentovascularis type IV
• Phacomatosis Melanorosea: A Further Case of an Unusual Skin Disorder
• Phacomatosis pigmento-pigmentaria: should we add a new type of phacomatosis? Fact and controversies
• Phacomatosis pigmentovascularis
• Phacomatosis Pigmentovascularis is Not a Twin-Spot Phenomenon
• Phacomatosis pigmentovascularis of cesioflammea type
• Phacomatosis pigmentovascularis spilorosea and mutation in the PTPN11 gene: new case with significant neurologic impairment
• Phacomatosis pigmentovascularis spilorosea mit Mutation im PTPN11 Gen: neuer Fall mit erheblichen neurologischen Beeintrachtigungen
• Phacomatosis pigmentovascularis type 2b (phacomatosis cesioflammea) with double superior vena cava, abdominal varicosities, and natal tooth: Novel associations
• Phacomatosis pigmentovascularis type IIa--case report
• Phacomatosis pigmentovascularis type IIB associated with Sturge-Weber syndrome: a case report and review of the literature
• Phacomatosis Pigmentovascularis Type Vb in a Three-Year Old Boy
• Phacomatosis pigmentovascularis with Raynaud's phenomena
• Phacomatosis pigmentovascularis with sturge-weber syndrome and congenital glaucoma: A rare case report
• Phacomatosis pigmentovascularis: Report of four new cases
• Phacomatosis Pigmentovascularis: Simple Presentation of a Not So Simple Dermatological Condition
• Phacomatosis spilorosea versus phacomatosis melanorosea: a critical reappraisal of the worldwide literature with updated classification of phacomatosis pigmentovascularis
• Phakomatosis Pigmentovascularis
• Phakomatosis Pigmentovascularis Associated With Sturge-Weber Syndrome, Ota Nevus, and Congenital Glaucoma
• Phakomatosis pigmentovascularis cesioflammea: a case report
• Phakomatosis pigmentovascularis Ib with left-sided hemihypertrophy, interdigital gaps and scoliosis: a unique case of phakomatosis pigmentovascularis
• Phakomatosis pigmentovascularis IIb (phakomatosis cesioflammea) associated with the absence of infrarenal inferior vena cava
• Phakomatosis pigmentovascularis type IIb
• Phakomatosis pigmentovascularis type IIb with Klippel-Trenaunay syndrome: Association with GNAQ mutation in vascular endothelial cells
• Phakomatosis pigmentovascularis Type IIb, Sturge-Weber syndrome and cone shaped tongue: An unusual association
• Phakomatosis pigmentovascularis type IIb: A case with Klippel-Trenáunay syndrome and extensive dermal melanocytosis as nevus of Ota, nevus of Ito and ectopic Mongolian spots
• Phakomatosis pigmentovascularis type Ⅲa mainly manifested by zosteriform nevus spilus: A case report with dermoscopic features
• Phakomatosis Pigmentovascularis: A Rare Disease
• Port-wine stain as a clue for two rare coexisting entities
• PTPN11 Mosaicism Causes a Spectrum of Pigmentary and Vascular Neurocutaneous Disorders and Predisposes to Melanoma
• Raynaud's Phenomenon and Limb Hypertrophy Presenting Phacomatosis Pigmentovascularis: A Rare Association
• Red-white and blue baby: a case of phacomatosis pigmentovascularis type V
• Retinal vascular abnormalities in a case of phakomatosis pigmentovascularis
• Retinal Vascular Abnormalities in Phakomatosis Pigmentovascularis
• Segmental hypomelanosis and hypermelanosis arranged in a checkerboard pattern are distinct naevi: flag-like hypomelanotic naevus and flag-like hypermelanotic naevus
• Sturge-Weber Syndrome Associated with Monolateral Ocular Melanocytosis, Iris Mammillations, and Diffuse Choroidal Haemangioma
• Sturge-Weber syndrome in association with Klippel-Trenaunay syndrome and phakomatosis pigmentovascularis type IIb
• Syndromes with vascular skin anomalies
• The case of a boy with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita: a unique instance of phacomatosis pigmentovascularis
• The risk of glaucoma associated with phacomatosis cesioflammea and phacomatosis cesioflammeo-marmorata
• Unusual case of phakomatosis pigmentovascularis in a Japanese female infant associated with three phakomatoses: Port-wine stain, dermal melanocytosis and cutis marmorata telangiectatica congenita
• Vascular and Pigmented Lesions of Phacomatosis Pigmentovascularis Treated With a Combination of Long-Pulsed, Q-Switched Laser, and Picosecond Lasers
• Vascular malformation and common keratinocytic nevus of the soft type: phacomatosis pigmentovascularis revisited