P Narcisi - JoVE Visualize

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Archives of Dermatology|May 1, 1985

Werner's syndrome. Biochemical and cytogenetic studiesD J Gawkrodger, G C Priestley, Vijayalaxmi, et al.

Lancet (London, England)|May 2, 1981

Some patients with cerebral aneurysms are deficient in type III collagenF M Pope, A C Nicholls, P Narcisi, et al.

Journal of Medical Genetics|June 1, 1992

Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IVL Nuytinck, P Narcisi, A Nicholls, et al.

American Journal of Medical Genetics|May 15, 1993

Single base mutation that substitutes glutamic acid for glycine 1021 in the COL3A1 gene and causes Ehlers-Danlos syndrome type IVP Narcisi, Y Wu, G Tromp, et al.

Human Genetics|June 1, 1992

A single base mutation in the gene for type III collagen (COL3A1) converts glycine 847 to glutamic acid in a family with Ehlers-Danlos syndrome type IV. An unaffected family member is mosaic for the mutationA J Richards, P N Ward, P Narcisi, et al.

Journal of Medical Genetics|July 1, 1991

Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IVA J Richards, J C Lloyd, P N Ward, et al.

Minerva Cardioangiologica|May 31, 2001

Personal experience of the treatment of ruptured aortic aneurysms. The prognostic evaluation of some parametersM Merlo, G Carignano, G Bitossi, et al.

Human Genetics|March 1, 1988

Linkage of a polymorphic marker for the type III collagen gene (COL3A1) to atypical autosomal dominant Ehlers-Danlos syndrome type IV in a large Belgian pedigreeA C Nicholls, A De Paepe, P Narcisi, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1988

Spontaneous carotid cavernous fistula in Ehlers Danlos syndromeR Fox, F M Pope, P Narcisi, et al.

The British Journal of Dermatology|July 1, 1987

Ehlers-Danlos syndrome type I: a clinical and ultrastructural study of a family with reduced amounts of collagen type IIIA De Paepe, A Nicholls, P Narcisi, et al.

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Showing results (11-20 of 21) with videos related to

Sort By:

Pageof 3

Archives of Dermatology|May 1, 1985

Werner's syndrome. Biochemical and cytogenetic studiesD J Gawkrodger, G C Priestley, Vijayalaxmi, et al.

Lancet (London, England)|May 2, 1981

Some patients with cerebral aneurysms are deficient in type III collagenF M Pope, A C Nicholls, P Narcisi, et al.

Journal of Medical Genetics|June 1, 1992

Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IVL Nuytinck, P Narcisi, A Nicholls, et al.

American Journal of Medical Genetics|May 15, 1993

Single base mutation that substitutes glutamic acid for glycine 1021 in the COL3A1 gene and causes Ehlers-Danlos syndrome type IVP Narcisi, Y Wu, G Tromp, et al.

Human Genetics|June 1, 1992

A single base mutation in the gene for type III collagen (COL3A1) converts glycine 847 to glutamic acid in a family with Ehlers-Danlos syndrome type IV. An unaffected family member is mosaic for the mutationA J Richards, P N Ward, P Narcisi, et al.

Journal of Medical Genetics|July 1, 1991

Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IVA J Richards, J C Lloyd, P N Ward, et al.

Minerva Cardioangiologica|May 31, 2001

Personal experience of the treatment of ruptured aortic aneurysms. The prognostic evaluation of some parametersM Merlo, G Carignano, G Bitossi, et al.

Human Genetics|March 1, 1988

Linkage of a polymorphic marker for the type III collagen gene (COL3A1) to atypical autosomal dominant Ehlers-Danlos syndrome type IV in a large Belgian pedigreeA C Nicholls, A De Paepe, P Narcisi, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1988

Spontaneous carotid cavernous fistula in Ehlers Danlos syndromeR Fox, F M Pope, P Narcisi, et al.

The British Journal of Dermatology|July 1, 1987

Ehlers-Danlos syndrome type I: a clinical and ultrastructural study of a family with reduced amounts of collagen type IIIA De Paepe, A Nicholls, P Narcisi, et al.

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