|1.||Valera, Elvis Terci: 2 articles (01/2012 - 02/2010)|
|2.||Scrideli, Carlos Alberto: 2 articles (01/2012 - 02/2010)|
|3.||Machado, Hélio Rubens: 2 articles (01/2012 - 02/2010)|
|4.||Oliveira, Ricardo Santos: 2 articles (01/2012 - 02/2010)|
|5.||Brassesco, María Sol: 2 articles (01/2012 - 02/2010)|
|6.||Tone, Luiz Gonzaga: 2 articles (01/2012 - 02/2010)|
|7.||Moog, U: 2 articles (11/2009 - 12/2005)|
|8.||Moog, Ute: 2 articles (12/2007 - 12/2007)|
|9.||Praticò, Andrea D: 1 article (12/2015)|
|10.||Ruggieri, Martino: 1 article (12/2015)|
|1.||Neurocutaneous Syndromes (Phakomatoses)
06/01/2014 - "Encephalocraniocutaneous lipomatosis is a rare neurocutaneous syndrome characterized by classical cutaneous and ocular lesions with central nervous system anomalies. "
05/01/2014 - "Encephalocraniocutaneous lipomatosis (ECCL) is a rare, sporadic congenital neurocutaneous disorder that characteristically involves ectomesodermal tissues, such as skin, eyes, and central nervous system. "
06/30/2013 - "Encephalocraniocutaneous lipomatosis (ECCL), also known as Haberland's Syndrome, is a sporadically occurring neurocutaneous syndrome with no gender or race predilection. "
05/01/2013 - "Encephalocraniocutaneous lipomatosis (ECCL) is a rare sporadic neurocutaneous syndrome characterized by presence of central nervous system, ocular and cutaneous anomalies. "
07/01/2011 - "Encephalocraniocutaneous lipomatosis (ECCL) is a rare neurocutaneous syndrome characterized by involvement of tissues of ectodermal and mesodermal origin such as skin, eye, adipose tissue, and brain. "
11/01/2002 - "The first case: A two-year-aged girl who had lipoma in quadrigeminal cistern and who suffered from encephalocraniocutaneous lipomatosis has been clinically studied. "
02/01/2002 - "Intracranial lipoma with extracranial extension through foramen ovale in a patient with encephalocraniocutaneous lipomatosis syndrome."
08/01/2000 - "The differential diagnosis to encephalocraniocutaneous lipomatosis with the typical finding of CNS lipoma is discussed."
04/01/1995 - "Encephalocraniocutaneous lipomatosis (ECCL) is a congenital hamartomatous disorder characterised by unilateral skin lesions, lipomas, and ipsilateral ophthamological and cerebral malformations. "
09/01/2011 - "Encephalocraniocutaneous lipomatosis (ECCL) is a rare neurocutaneous syndrome whose hallmark lesions are benign lipomas of the brain and spinal cord. "
12/01/2014 - "Nevus sebaceus may be a cutaneous marker for several complex syndromes whereas nevus psiloliparus presents almost always in connection with encephalocraniocutaneous lipomatosis. "
11/01/2014 - "Nevus psiloliparus is a type of mesodermal nevus of the scalp classically seen with encephalocraniocutaneous lipomatosis. "
05/01/2011 - "[Nevus psiloliparus in a child with encephalocraniocutaneous lipomatosis]."
01/01/1998 - "In particular, nevus psiloliparus can be separated from the Hoffmann-Zurhelle nevus that has so far never been observed in cases of encephalocraniocutaneous lipomatosis. "
01/01/1998 - "A comprehensive comparison shows that nevus psiloliparus can be distinguished from other types of fatty tissue nevi by clinical criteria such as localization on the scalp, a flat smooth surface and absence of hair follicles, by the histopathological feature of isolated arrector pili muscles and by the presence of associated extracutaneous features in the form of encephalocraniocutaneous lipomatosis. "
11/01/1993 - "The literature relating to encephalocraniocutaneous lipomatosis is reviewed, as well as that relating to the syndromes of naevus unius lateris, the Proteus syndrome and the syndrome of cranial hemihypertrophy, and the clinical features of our two cases are compared with the features of these four syndromes."
10/01/1993 - "We report on a patient with manifestations of encephalocraniocutaneous lipomatosis and Proteus syndrome. "
10/01/1993 - "Encephalocraniocutaneous lipomatosis, Proteus syndrome, and somatic mosaicism."
07/01/1992 - "We compared our findings in these three patients with those of 50 others with Proteus syndrome and nine with encephalocraniocutaneous lipomatosis (ECCL) reported in the literature. "
07/01/1992 - "Encephalocraniocutaneous lipomatosis and the Proteus syndrome: distinct entities with overlapping manifestations."
|5.||Congenital, Hereditary, and Neonatal Diseases and Abnormalities (Congenital Disorders)
08/01/2005 - "Encephalocraniocutaneous lipomatosis is a rare congenital disorder characterized by an abnormal development of adipose tissue, and is of unknown pathogenesis. "
08/20/1999 - "Encephalocraniocutaneous lipomatosis (ECCL) is a rare congenital disorder and was first described in 1970. "
06/01/1993 - "Encephalocraniocutaneous lipomatosis is a congenital disorder characterized by unilateral cerebral malformations and ipsilateral scalp, face, and eye lesions. "
12/01/2014 - "Encephalocraniocutaneous lipomatosis (ECCL, Haberland syndrome, Fishman syndrome) is a very rare congenital disorder, involving skin, eye, bone and central nervous system malformations. "
|8.||syndromic 7 Microphthalmia
|9.||Wyburn Mason's syndrome