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LYMPHODYSPLASIA AND KRAS MUTATION: A CASE REPORT AND LITERATURE REVIEW

Lymphology, 2015-09, Vol.48 (3), p.121-127

2015

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Dynamics of pleural fluid effusion and chylothorax in the fetus and newborn: role of the lymphatic system

Lymphology, 2013-06, Vol.46 (2), p.75-84

2013

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Congenital fetal and neonatal visceral chylous effusions: neonatal chylothorax and chylous ascites revisited. A multicenter retrospective study

Lymphology, 2012-09, Vol.45 (3), p.91-102

2012

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Lymphoscintigraphy patterns in newborns and children with congenital lymphatic dysplasia

Lymphology, 2014-03, Vol.47 (1), p.28-39

2014

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Are there lymphatic vessels in the placenta?

Lymphology, 2012-03, Vol.45 (1), p.34-36

2012

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Lymphodynamics in the fetus and newborn

Lymphology, 2006-09, Vol.39 (3), p.110-117

2006

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Lymphoscintigraphy in paediatric patients

Phlebology, 2009-10, Vol.24 (5), p.237; author reply 238-237

2009

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Perinatal deaths and lymphatic system involvement: a diagnostic flow-chart applying immunohistochemical methods

Lymphology, 2011-09, Vol.44 (3), p.131-133

2011

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Congenital lymphatic dysplasia in Kabuki syndrome: first report of an unusual association

Lymphology, 2010-12, Vol.43 (4), p.188-191

2010

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Congenital lymphatic dysplasias: genetics review and resources for the lymphologist

Lymphology, 2009-03, Vol.42 (1), p.36-41

2009

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The role of lymphoscintigraphy in the diagnosis of lymphedema in Turner syndrome

Lymphology, 2009-09, Vol.42 (3), p.123-129

2009

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Immunohistochemical studies in a hydroptic fetus with pulmonary lymphangiectasia and trisomy 21

Lymphology, 2007-09, Vol.40 (3), p.114-121

2007

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Selective D2-40 lymphatic endothelium immunoreactivity in developing human fetal skin appendages

Lymphology, 2009-06, Vol.42 (2), p.61-65

2009

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Pulmonary lymphangiectasia

Lymphology, 2005-09, Vol.38 (3), p.111-121

2005

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Sebaceous nevus syndrome: Report of two cases

Pediatric neurology, 1997-07, Vol.17 (1), p.77-79

1997

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Fumarate hydratase deficiency

Journal of inherited metabolic disease, 1998-06, Vol.21 (4), p.435-436

1998

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Nonimmune idiopathic hydrops fetalis and congenital lymphatic dysplasia

American journal of medical genetics. Part A, 2006-04, Vol.140A (7), p.678-684

2006

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Heterozygous mutations of growth hormone receptor gene in children with idiopathic short stature

Growth hormone & IGF research, 2005-12, Vol.15 (6), p.405-410

2005

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SELECTIVE D2-40 LYMPHATIC ENDOTHELIUM IMMUNOREACTIVITY IN DEVLOPING HUMAN FETAL SKIN APPENDAGES

Lymphology, 2009-06, Vol.42 (2), p.61-65

2009

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Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome

Genetic counseling, 1995, Vol.6 (4), p.309

1995

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Phenobarbital Enhances Sister Chromatid Exchanges In Vivo

Epilepsia (Copenhagen), 2003-04, Vol.44 (4), p.621-622

2003

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Lymohodynamics in the fetus and newborn

Lymphology, 2006, Vol.39 (3), p.110-117

2006

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Aplasia cutis congenita, skull defect, brain heterotopia, and intestinal lymphangiectasia

American journal of medical genetics. Part A, 2005-01, Vol.132A (2), p.202-205

2005

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Combined deficiency of xanthine oxidase and sulphite oxidase due to a deficiency of molybdenum cofactor

Journal of inherited metabolic disease, 1996-01, Vol.19 (5), p.700-701

1996

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The Genoa experience of prenatal diagnosis in NF1

Prenatal diagnosis, 2000-09, Vol.20 (9), p.719-724

2000

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LYMPHODYSPLASIA AND KRAS MUTATION: A CASE REPORT AND LITERATURE REVIEW

Dynamics of pleural fluid effusion and chylothorax in the fetus and newborn: role of the lymphatic system

Congenital fetal and neonatal visceral chylous effusions: neonatal chylothorax and chylous ascites revisited. A multicenter retrospective study

Lymphoscintigraphy patterns in newborns and children with congenital lymphatic dysplasia

Are there lymphatic vessels in the placenta?

Lymphodynamics in the fetus and newborn

Lymphoscintigraphy in paediatric patients

Perinatal deaths and lymphatic system involvement: a diagnostic flow-chart applying immunohistochemical methods

Congenital lymphatic dysplasia in Kabuki syndrome: first report of an unusual association

Congenital lymphatic dysplasias: genetics review and resources for the lymphologist

The role of lymphoscintigraphy in the diagnosis of lymphedema in Turner syndrome

Immunohistochemical studies in a hydroptic fetus with pulmonary lymphangiectasia and trisomy 21

Selective D2-40 lymphatic endothelium immunoreactivity in developing human fetal skin appendages

Pulmonary lymphangiectasia

Sebaceous nevus syndrome: Report of two cases

Fumarate hydratase deficiency

Nonimmune idiopathic hydrops fetalis and congenital lymphatic dysplasia

Heterozygous mutations of growth hormone receptor gene in children with idiopathic short stature

SELECTIVE D2-40 LYMPHATIC ENDOTHELIUM IMMUNOREACTIVITY IN DEVLOPING HUMAN FETAL SKIN APPENDAGES

Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome

Phenobarbital Enhances Sister Chromatid Exchanges In Vivo

Lymohodynamics in the fetus and newborn

Aplasia cutis congenita, skull defect, brain heterotopia, and intestinal lymphangiectasia

Combined deficiency of xanthine oxidase and sulphite oxidase due to a deficiency of molybdenum cofactor

The Genoa experience of prenatal diagnosis in NF1

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