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Propranolol targets the contractility of infantile haemangioma-derived pericytes

British journal of dermatology (1951), 2014-11, Vol.171 (5), p.1129-1137

2014

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Safety and Clinical Efficacy of Onyx for Embolization of Extracranial Head and Neck Vascular Anomalies

American journal of neuroradiology : AJNR, 2011-06, Vol.32 (6), p.1082-1086

2011

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Complex Spinal-Paraspinal Fast-Flow Lesions in CLOVES Syndrome: Analysis of Clinical and Imaging Findings in 6 Patients

American journal of neuroradiology : AJNR, 2011-11, Vol.32 (10), p.1812-1817

2011

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A Novel Association between RASA1 Mutations and Spinal Arteriovenous Anomalies

American journal of neuroradiology : AJNR, 2010-04, Vol.31 (4), p.775-779

2010

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Recessive primary congenital lymphoedema caused by a VEGFR3 mutation

Journal of medical genetics, 2009-06, Vol.46 (6), p.399-404

2009

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Spastic diplegia as a complication of interferon Alfa-2a treatment of hemangiomas of infancy

The Journal of pediatrics, 1998-03, Vol.132 (3), p.527-530

1998

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Intracranial Vascular Anomalies in Patients with Periorbital Lymphatic and Lymphaticovenous Malformations

American Journal of Neuroradiology, 2007-02, Vol.28 (2), p.335-341

2007

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Infantile Hemangiomas Involving the Neuraxis: Clinical and Imaging Findings

American journal of neuroradiology : AJNR, 2009-05, Vol.30 (5), p.1005-1013

2009

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Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations

Clinical genetics, 2006-10, Vol.70 (4), p.330-335

2006

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Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia

Cell, 1997-05, Vol.89 (5), p.773-779

1997

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Soft-tissue vascular anomalies: utility of US for diagnosis

Radiology, 2000-03, Vol.214 (3), p.747

2000

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Mutation Analysis of Core Binding Factor A1 in Patients with Cleidocranial Dysplasia

American journal of human genetics, 1999-11, Vol.65 (5), p.1268-1278

1999

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Analysis of Posterior Plagiocephaly: Deformational versus Synostotic

Plastic and reconstructive surgery (1963), 1999-02, Vol.103 (2), p.371-380

1999

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Noninvoluting Congenital Hemangioma: A Rare Cutaneous Vascular Anomaly

Plastic and reconstructive surgery (1963), 2001-06, Vol.107 (7), p.1647-1654

2001

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Hermann Friedberg's case report: an early description of CLOVES syndrome

Clinical genetics, 2010-10, Vol.78 (4), p.342-347

2010

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Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis

Human molecular genetics, 2000-03, Vol.9 (5), p.765-768

2000

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Four common glomulin mutations cause two thirds of glomuvenous malformations (“familial glomangiomas”): evidence for a founder effect

Journal of medical genetics, 2005-02, Vol.42 (2), p.e13-e13

2005

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Complications of systemic corticosteroid therapy for problematic hemangioma

Plastic and reconstructive surgery (1963), 1999-11, Vol.104 (6), p.1616-1623

1999

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The principle of rotation advancement for repair of unilateral complete cleft lip and nasal deformity : Technical variations and analysis of results

Plastic and reconstructive surgery (1963), 1999-10, Vol.104 (5), p.1247-1260

1999

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Antiangiogenic therapy of a recurrent giant cell tumor of the mandible with interferon alfa-2a

Pediatrics (Evanston), 1999-06, Vol.103 (6 Pt 1), p.1145

1999

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Thrombocytopenic coagulopathy (Kasabach-Merritt phenomenon) is associated with kaposiform hemangioendothelioma and not with common infantile hemangioma

Plastic and reconstructive surgery (1963), 1997-11, Vol.100 (6), p.1377-1386

1997

Volltextzugriff (PDF)

Residual lesions after Kasabach-Merritt phenomenon in 41 patients

Journal of the American Academy of Dermatology, 2000-02, Vol.42 (2), p.225-235

2000

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Interferon Alfa-2a Therapy for Life-Threatening Hemangiomas of Infancy

The New England journal of medicine, 1992-05, Vol.326 (22), p.1456-1463

1992

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Prenatal diagnosis of cleft lip and cleft palate using MRI

American journal of roentgenology (1976), 2004-07, Vol.183 (1), p.229

2004

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Cerebral vasculopathy and neurologic sequelae in infants with cervicofacial hemangioma: report of eight patients

Radiology, 1998-06, Vol.207 (3), p.601

1998

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Propranolol targets the contractility of infantile haemangioma-derived pericytes

Safety and Clinical Efficacy of Onyx for Embolization of Extracranial Head and Neck Vascular Anomalies

Complex Spinal-Paraspinal Fast-Flow Lesions in CLOVES Syndrome: Analysis of Clinical and Imaging Findings in 6 Patients

A Novel Association between RASA1 Mutations and Spinal Arteriovenous Anomalies

Recessive primary congenital lymphoedema caused by a VEGFR3 mutation

Spastic diplegia as a complication of interferon Alfa-2a treatment of hemangiomas of infancy

Intracranial Vascular Anomalies in Patients with Periorbital Lymphatic and Lymphaticovenous Malformations

Infantile Hemangiomas Involving the Neuraxis: Clinical and Imaging Findings

Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations

Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia

Soft-tissue vascular anomalies: utility of US for diagnosis

Mutation Analysis of Core Binding Factor A1 in Patients with Cleidocranial Dysplasia

Analysis of Posterior Plagiocephaly: Deformational versus Synostotic

Noninvoluting Congenital Hemangioma: A Rare Cutaneous Vascular Anomaly

Hermann Friedberg's case report: an early description of CLOVES syndrome

Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis

Four common glomulin mutations cause two thirds of glomuvenous malformations (“familial glomangiomas”): evidence for a founder effect

Complications of systemic corticosteroid therapy for problematic hemangioma

The principle of rotation advancement for repair of unilateral complete cleft lip and nasal deformity : Technical variations and analysis of results

Antiangiogenic therapy of a recurrent giant cell tumor of the mandible with interferon alfa-2a

Thrombocytopenic coagulopathy (Kasabach-Merritt phenomenon) is associated with kaposiform hemangioendothelioma and not with common infantile hemangioma

Residual lesions after Kasabach-Merritt phenomenon in 41 patients

Interferon Alfa-2a Therapy for Life-Threatening Hemangiomas of Infancy

Prenatal diagnosis of cleft lip and cleft palate using MRI

Cerebral vasculopathy and neurologic sequelae in infants with cervicofacial hemangioma: report of eight patients

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