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Propranolol and prednisolone combination for the treatment of segmental haemangioma in PHACES syndrome

British journal of dermatology (1951), 2015-07, Vol.173 (1), p.242-246

2015

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Mitochondrial DNA haplogroups may influence Fabry disease phenotype

Neuroscience letters, 2016-08, Vol.629, p.58-61

2016

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Effect of Lactobacillus reuteri (DSM 17938) on methane production in patients affected by functional constipation: a retrospective study

European review for medical and pharmacological sciences, 2017-04, Vol.21 (7), p.1702

2017

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Angiokeratoma: decision-making aid for the diagnosis of Fabry disease

British journal of dermatology (1951), 2012-04, Vol.166 (4), p.712-720

2012

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First report of hereditary Christ-Siemens-Touraine syndrome and non-segmental vitiligo association in a young adult: contraindication for vitiligo treatment

Journal of the European Academy of Dermatology and Venereology, 2016-02, Vol.30 (2), p.346-348

2016

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A Case of Pyoderma Gangrenosum After Long Saphenous Vein Harvesting

European journal of vascular and endovascular surgery, 2014-03, Vol.47 (3), p.330-330

2014

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Mutation identification of Fabry disease in families with other lysosomal storage disorders

Clinical genetics, 2013-09, Vol.84 (3), p.281-285

2013

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Propranolol for infantile haemangiomas: single centre experience of 250 cases and proposed therapeutic protocol

Archives of disease in childhood, 2014-12, Vol.99 (12), p.1132-1136

2014

Volltextzugriff (PDF)

860 Understanding cellular & molecular responses in the treatment of pediatric lymphatic anomalies

Journal of investigative dermatology, 2017-05, Vol.137 (5), p.S148-S148

2017

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088 Antiproliferative effect of propranolol on Lymphatic Malformations

Journal of investigative dermatology, 2016-09, Vol.136 (9), p.S175-S175

2016

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Multiplex Laser for treating Non Involuting Congenital Haemangiomas (NICH) in children

Journal of Pakistan Association of Dermatologists : JPAD, 2019-09, Vol.29 (3), p.274

2019

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Reversed palmaris longus muscle: Anatomical variant - case report and literature review

Canadian journal of plastic surgery, 2013-03, Vol.21 (1), p.55-56

2013

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Angiokeratoma: decision-making aid for the diagnosis of Fabry disease: Angiokeratoma, proposal for a diagnostic algorithm

British journal of dermatology (1951), 2012-04, Vol.166 (4), p.712-720

2012

Volltextzugriff (PDF)

Angiokeratoma: Decision Making Methodology for the Diagnosis of Fabry Disease

British journal of dermatology (1951), 2011-11, p.no-no

2011

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A Case of Pyoderma Gangrenosum After Long Saphenous Vein Harvesting

European journal of vascular and endovascular surgery extra, 2014-02, Vol.27 (2), p.e5-e6

2014

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Efficacy, perception, and utilization of pediatric teledermatology: A systematic reviewCapsule Summary

JAAD international, 2023-09, Vol.12, p.3-11

2023

Volltextzugriff (PDF)

Propranolol and prednisolone combination for the treatment of segmental haemangioma in PHACES syndrome

British Journal of Dermatology, 2015, Vol.173 (1), p.242-246

2015

Volltextzugriff (PDF)

First report of hereditary Christ-Siemens-Touraine syndrome and non-segmental vitiligo association in a young adult: contraindication for vitiligo treatment

Journal of the European Academy of Dermatology and Venereology : JEADV, 2016, Vol.30 (2), p.346-348

2016

Volltextzugriff (PDF)

Unobtrusive monitoring of Restless Legs and periodic leg movements during sleep using a sensorized mattress

Sleep medicine, 2024-02, Vol.115, p.420-420

2024

Volltextzugriff (PDF)

Mutations of the VHL tumour suppressor gene in renal carcinoma

Nature genetics, 1994-05, Vol.7 (1), p.85-90

1994

Volltextzugriff (PDF)

Allelic deletions of the VHL gene detected in multiple microscopic clear cell renal lesions in von Hippel-Lindau disease patients

The American journal of pathology, 1996-12, Vol.149 (6), p.2089-2094

1996

Volltextzugriff (PDF)

Unique functions for Notch4 in murine embryonic lymphangiogenesis

Angiogenesis (London), 2022-05, Vol.25 (2), p.205-224

2022

Volltextzugriff (PDF)

Defective Placental Vasculogenesis Causes Embryonic Lethality in VHL-Deficient Mice

Proceedings of the National Academy of Sciences - PNAS, 1997-08, Vol.94 (17), p.9102-9107

1997

Volltextzugriff (PDF)

Role of Transforming Growth Factor-α in von Hippel-Lindau (VHL)-/-Clear Cell Renal Carcinoma Cell Proliferation: A Possible Mechanism Coupling VHL Tumor Suppressor Inactivation and Tumorigenesis

Proceedings of the National Academy of Sciences - PNAS, 2001-02, Vol.98 (4), p.1387-1392

2001

Volltextzugriff (PDF)

CLINICAL AND GENETIC CHARACTERIZATION OF PHEOCHROMOCYTOMA IN VON HIPPEL-LINDAU FAMILIES: COMPARISON WITH SPORADIC PHEOCHROMOCYTOMA GIVES INSIGHT INTO NATURAL HISTORY OF PHEOCHROMOCYTOMA

The Journal of urology, 1999-09, Vol.162 (3), p.659-664

1999

Volltextzugriff (PDF)

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Propranolol and prednisolone combination for the treatment of segmental haemangioma in PHACES syndrome

Mitochondrial DNA haplogroups may influence Fabry disease phenotype

Effect of Lactobacillus reuteri (DSM 17938) on methane production in patients affected by functional constipation: a retrospective study

Angiokeratoma: decision-making aid for the diagnosis of Fabry disease

First report of hereditary Christ-Siemens-Touraine syndrome and non-segmental vitiligo association in a young adult: contraindication for vitiligo treatment

A Case of Pyoderma Gangrenosum After Long Saphenous Vein Harvesting

Mutation identification of Fabry disease in families with other lysosomal storage disorders

Propranolol for infantile haemangiomas: single centre experience of 250 cases and proposed therapeutic protocol

860 Understanding cellular & molecular responses in the treatment of pediatric lymphatic anomalies

088 Antiproliferative effect of propranolol on Lymphatic Malformations

Multiplex Laser for treating Non Involuting Congenital Haemangiomas (NICH) in children

Reversed palmaris longus muscle: Anatomical variant - case report and literature review

Angiokeratoma: decision-making aid for the diagnosis of Fabry disease: Angiokeratoma, proposal for a diagnostic algorithm

Angiokeratoma: Decision Making Methodology for the Diagnosis of Fabry Disease

A Case of Pyoderma Gangrenosum After Long Saphenous Vein Harvesting

Efficacy, perception, and utilization of pediatric teledermatology: A systematic reviewCapsule Summary

Propranolol and prednisolone combination for the treatment of segmental haemangioma in PHACES syndrome

First report of hereditary Christ-Siemens-Touraine syndrome and non-segmental vitiligo association in a young adult: contraindication for vitiligo treatment

Unobtrusive monitoring of Restless Legs and periodic leg movements during sleep using a sensorized mattress

Mutations of the VHL tumour suppressor gene in renal carcinoma

Allelic deletions of the VHL gene detected in multiple microscopic clear cell renal lesions in von Hippel-Lindau disease patients

Unique functions for Notch4 in murine embryonic lymphangiogenesis

Defective Placental Vasculogenesis Causes Embryonic Lethality in VHL-Deficient Mice

Role of Transforming Growth Factor-α in von Hippel-Lindau (VHL)-/-Clear Cell Renal Carcinoma Cell Proliferation: A Possible Mechanism Coupling VHL Tumor Suppressor Inactivation and Tumorigenesis

CLINICAL AND GENETIC CHARACTERIZATION OF PHEOCHROMOCYTOMA IN VON HIPPEL-LINDAU FAMILIES: COMPARISON WITH SPORADIC PHEOCHROMOCYTOMA GIVES INSIGHT INTO NATURAL HISTORY OF PHEOCHROMOCYTOMA

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