(Q36980361)

17 August 2017

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title

Multiple cerebral cavernous malformations associated with extracranial mesenchymal anomalies (English)

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17 August 2017

Ardavan Ardeshiri

1

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17 August 2017

Ardeshir Ardeshiri

2

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17 August 2017

Andres Beiras-Fernandez

3

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17 August 2017

Ortrud K Steinlein

4

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17 August 2017

Peter A Winkler

5

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17 August 2017

language of work or name

1 reference

24 October 2007

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17 August 2017

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17 August 2017

volume

31

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17 August 2017

issue

1

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17 August 2017

page(s)

11-7; discussion 17-8

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17 August 2017

cites work

Familial Atrial Myxoma

1 reference

https://api.crossref.org/works/10.1007%2FS10143-007-0111-7

Neurologic manifestations of atrial myxoma. A 12-year experience and review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10143-007-0111-7

Vascular malformations and epilepsy: clinical considerations and basic mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10143-007-0111-7

Left Atrial Myxoma as a Neurological Problem: A Case Report and Review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10143-007-0111-7

[131 cases of cavernous angioma (cavernomas) of the CNS, discovered by retrospective analysis of 24,535 autopsies]

21 January 2018

1 reference

12 December 2020

Spinal cord cavernous malformation in a patient with familial intracranial cavernous malformations

1 reference

12 December 2020

An association between autosomal dominant cerebral cavernomas and a distinctive hyperkeratotic cutaneous vascular malformation in 4 families.

1 reference

12 December 2020

Mutations within the MGC4607 gene cause cerebral cavernous malformations

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12 December 2020

Cavernous malformations of the brain stem. A review of 139 cases

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12 December 2020

Update on the molecular genetics of vascular anomalies

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12 December 2020

Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex.

1 reference

12 December 2020

Cavernous hemangioma of the retina, cutaneous angiomas, and intracranial vascular lesion by computed tomography and nuclear magnetic resonance imaging

1 reference

12 December 2020

Mixed vascular malformations of the brain: clinical and pathogenetic considerations.

1 reference

12 December 2020

The natural history of familial cavernous malformations: results of an ongoing study

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12 December 2020

santa and valentine pattern concentric growth of cardiac myocardium in the zebrafish

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12 December 2020

[Familial cerebral cavernomatosis associated with cutaneous angiomas]

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12 December 2020

Value of gradient-echo magnetic resonance imaging in the diagnosis of familial cerebral cavernous malformation.

1 reference

12 December 2020

Tumors and the heart: molecular genetic advances

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12 December 2020

The natural history of familial cerebral cavernomas: a retrospective MRI study of 40 patients

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12 December 2020

CCM1 gene deletion identified by MLPA in cerebral cavernous malformation.

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12 December 2020

Genetics of cavernous angiomas

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12 December 2020

Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complex.

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12 December 2020

1 reference

12 December 2020

Ultrastructural pathological features of cerebrovascular malformations: a preliminary report.

1 reference

12 December 2020

Cerebral cavernomas in the adult. Review of the literature and analysis of 72 surgically treated patients

1 reference

12 December 2020

Cavernous malformation within a schwannoma: review of the literature and hypothesis of a common genetic etiology

1 reference

12 December 2020

The natural history of cavernous malformations.

1 reference

12 December 2020

Cerebral cavernous malformation: new molecular and clinical insights

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12 December 2020

The association of extracranial and intracranial vascular malformations in children

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12 December 2020

Intracranial aneurysm associated with cerebral cavernous angioma. Case report.

1 reference

12 December 2020

Diffuse liver angiosarcoma and cerebral cavernous angiomas in a young patient.

1 reference

12 December 2020

The complex of myxomas, spotty pigmentation, and endocrine overactivity

1 reference

12 December 2020

Mutational analysis of 206 families with cavernous malformations.

1 reference

12 December 2020

[A case of familial cardiac myxoma]

1 reference

12 December 2020

Familial cerebral, hepatic, and retinal cavernous angiomas

1 reference

12 December 2020

Cerebral cavernous malformations and epilepsy

1 reference

12 December 2020

Delayed neurologic complications of left atrial myxoma.

1 reference

12 December 2020

Biallelic somatic and germ line CCM1 truncating mutations in a cerebral cavernous malformation lesion.

1 reference

12 December 2020

Patients with spinal cord cavernous malformations are at an increased risk for multiple neuraxis cavernous malformations

1 reference

12 December 2020

Cerebral metastasis of an atrial myxoma mimicking an epithelioid hemangioendothelioma.

1 reference

12 December 2020

A syndrome of various cutaneous pigmented lesions, myxoid neurofibromata and atrial myxoma: the NAME syndrome

1 reference

12 December 2020

Mucocutaneous lentigines, cardiomucocutaneous myxomas, and multiple blue nevi: the "LAMB" syndrome

1 reference

12 December 2020

Cavernomas in the central nervous system and the relevance of multiple intracranial lesions in the familial form of this disease

1 reference

12 December 2020

Genetics of cerebral cavernous angioma

1 reference

12 December 2020

Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Société Française de Neurochirurgie.

1 reference

12 December 2020

Ultrastructural and immunocytochemical evidence that an incompetent blood-brain barrier is related to the pathophysiology of cavernous malformations

1 reference

12 December 2020

The natural history of cerebral cavernous malformations

1 reference

12 December 2020

Cardiac myxoma. A clinicopathologic study

1 reference

12 December 2020

Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 11-2002. A 27-year-old woman with two intracardiac masses and a history of endocrinopathy

1 reference

12 December 2020

A novel gene mutation (1292 deletion) in a Chinese family with cerebral cavernous malformations

1 reference

12 December 2020

[Multiple and familial cavernous angiomas in the brain and extremities--case report]

1 reference

12 December 2020

Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families

1 reference

12 December 2020

Cavernous malformations and capillary telangiectasia: a spectrum within a single pathological entity

1 reference

12 December 2020

An analysis of the natural history of cavernous angiomas.

1 reference

12 December 2020

Large germline deletions and duplication in isolated cerebral cavernous malformation patients.

1 reference

12 December 2020

Familial multiple cavernous angioma in the brain and spinal cord

1 reference

12 December 2020

Familial cavernous malformations of the central nervous system and retina

1 reference

12 December 2020

Cardiac myxoma metastasized to the brain: potential role of endogenous interleukin-6.

1 reference

12 December 2020

Multiple cerebral aneurysms as delayed complication of left cardiac myxoma: a case report and review

1 reference

12 December 2020

CCM1 and CCM2 protein interactions in cell signaling: implications for cerebral cavernous malformations pathogenesis

1 reference

12 December 2020

Cavernous angiomas of the brain. Account of fourteen personal cases and review of the literature

1 reference

12 December 2020

Structural features of cardiac myxomasHistology, histochemistry, and electron microscopy

1 reference

12 December 2020

Familial cardiac myxoma--a comprehensive review of reported cases.

1 reference

12 December 2020

10.1007/S10143-007-0111-7

Identifiers

DOI

1 reference

release_zi6i7rtkmzfazco3rjfufkhebe

17 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/zi6i7rtkmzfazco3rjfufkhebe

24 November 2022

mapped directly with Wikidata item

1 reference