|1.||Happle, Rudolf: 5 articles (07/2012 - 11/2003)|
|2.||Happle, R: 4 articles (11/2015 - 06/2003)|
|3.||Grammatico, Paola: 2 articles (09/2011 - 02/2008)|
|4.||Castori, Marco: 2 articles (09/2011 - 02/2008)|
|5.||Praticò, Andrea D: 1 article (12/2015)|
|6.||Ruggieri, Martino: 1 article (12/2015)|
|7.||Torchia, D: 1 article (11/2015)|
|8.||Surjana, Devita: 1 article (06/2015)|
|9.||Zappala, Tania: 1 article (06/2015)|
|10.||Yoong, Corinne: 1 article (06/2015)|
06/01/2015 - "Phacomatosis pigmentovascularis is a rare genodermatosis characterized by the combination of an extensive pigmentary nevus with a widespread vascular nevus. "
11/01/2013 - "Phacomatosis Pigmentovascularis is a rare syndrome characterized by capillary malformation and pigmentary nevus. "
01/01/2013 - "Phacomatosis pigmentovascularis (PPV) is an association of vascular nevus with pigmentary nevus. "
03/01/2010 - "The term phacomatosis pigmentovascularis (PPV) refers to the occurrence of vascular nevi with melanocytic or epidermal nevi. "
09/01/2007 - "Phacomatosis pigmentovascularis (PPV) is a group of syndromes comprising coexistent vascular and pigmentary nevi, which is first classified into five subtypes and then further categorized according to the absence or presence of associated systemic findings as type (a) and (b), respectively. "
|2.||Port-Wine Stain (Nevus Flammeus)
11/01/2013 - "A case of a 2-year-old patient is reported, who presented extensive nevus flammeus and an aberrant Mongolian spot, without systemic disease, manifestations that allow us to classify this case as type IIa Phacomatosis Pigmentovascularis, according to Hasegawa's classification."
06/01/2011 - "Phacomatosis pigmentovascularis shows features of nevus flammeus and more serious ocular pigmentary abnormalities (uveoscleral melanocytosis and conjunctival melanosis). "
11/01/1987 - "The capillary vessels are ultrastructurally different in phacomatosis pigmentovascularis from those of a nevus flammeus in the Sturge-Weber syndrome; however, melanocytes of normal aspect were present in the middle and deep dermis. "
01/01/2013 - "In the first of two cases reported here, a 2-week-old Japanese baby girl was given a diagnosis of phacomatosis pigmentovascularis type II and Klippel-Trénaunay syndrome because of port-wine stains, cutis marmorata telangiectatica congenita, and aberrant Mongolian spots over her trunk and limbs. "
06/01/2011 - "All patients with nevus flammeus should be examined for phacomatosis pigmentovascularis by an ophthalmologist because ocular melanocytosis and uveal melanoma may remain hidden within the eye."
|3.||Neurocutaneous Syndromes (Phakomatoses)
11/01/2015 - "Ten cases belonged to phacomatosis melanorosea, whereas several others were part of so far uncategorized cases of phacomatosis pigmentovascularis. "
07/01/2012 - "Phacomatosis melanorosea without extracutaneous features: an unusual type of phacomatosis pigmentovascularis."
12/01/2011 - "Phacomatosis pigmentovascularis and extensive venous malformation of brain vessels: an unknown association or a new vascular neurocutaneous syndrome?"
11/01/2007 - "Phacomatosis spilorosea (phacomatosis pigmentovascularis type IIIb)."
03/01/2006 - "This association of CMTC with Mongolian spots has been reported as a distinct type of phacomatosis pigmentovascularis (PPV), namely PPV type V. More recently, the term phacomatosis cesiomarmorata (cesius = blue) has been proposed. "
05/01/2015 - "Phacomatosis pigmentovascularis is a rare, congenital condition characterized by a combination of cutaneous melanocytic lesions and vascular malformation. "
12/01/1998 - "Phacomatosis pigmentovascularis (PPV) is described as the association of cutaneous vascular malformations and different pigmentary disorders. "
01/01/2014 - "Phacomatosis pigmentovascularis is a rare syndrome characterized by the coexistence of a pigmented nevus and a cutaneous vascular malformation. "
01/01/2014 - "Vascular malformation and common keratinocytic nevus of the soft type: phacomatosis pigmentovascularis revisited."
09/10/2013 - "An 8-month-old boy with cutaneous vascular malformations and dermal melanocytosis (Mongolian spots, figure, A) on the face and trunk was diagnosed with phacomatosis pigmentovascularis type 2. He had normal neurodevelopment, but progressive macrocephaly (figure, B). "
|5.||Sturge-Weber Syndrome (Sturge-Kalischer-Weber Syndrome)
01/01/2013 - "Phacomatosis pigmentovascularis type IIB associated with Sturge-Weber syndrome: a case report and review of the literature."
05/01/2010 - "To the best of our knowledge, this is the second infantile case meeting diagnostic criteria for systemic phacomatosis pigmentovascularis type IIb, Sturge-Weber syndrome and Klippel-Trenaunay syndrome in the English language literature."
05/01/2010 - "We present two rare cases of phacomatosis pigmentovascularis type IIb, with one patient demonstrating concurrent Sturge-Weber syndrome and Klippel-Trenaunay syndrome. "
05/01/2010 - "Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome."
08/01/2007 - "A case of Sturge-Weber syndrome in association with phacomatosis pigmentovascularis and developmental glaucoma."
|2.||Cutis marmorata telangiectatica congenita
|8.||Wyburn Mason's syndrome
|10.||Blue rubber bleb nevus syndrome