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Cristina Nolla Fontana

Cristina Nolla Fontana

Institutions of which they are part

Predoctoral researcher
Systemic Diseases
Vall Hebron Institut de Recerca
Cristina Nolla Fontana

Cristina Nolla Fontana

Cristina Nolla Fontana

Institutions of which they are part

Predoctoral researcher
Systemic Diseases
Vall Hebron Institut de Recerca

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Equip de Vall d'Hebron que ha liderat l'estudi

A genomic technique reveals a new genetic alteration in hereditary angioedema

A Vall d’Hebron team demonstrates, for the first time, the potential of optical genome mapping to detect genetic alterations associated with this rare disease that are not identified using conventional methods.

Vall d'Hebron team

Identified several cases of a rare disease transmitted by a sperm donor

The study describes the first documented case worldwide of hereditary angioedema transmission through assisted reproduction.

Eular-Antonio-Cano

Strong presence of VHIR at the European Alliance of Associations for Rheumatology Congress

15 researchers from the Rheumatology, Systemic Diseases and the Physiology and Pathophysiology of the Digestive Tract groups gave around 25 presentations.

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