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Blogadmin2022-07-29T15:37:05+02:00

Cardiological aspects highlighted in patients with COL4A1-A2
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Cardiological aspects highlighted in patients with COL4A1-A2

admin2024-10-18T07:18:31+02:0018/10/2024|News, Resources|

The COL4A1/COL4A2 ocular phenotypic spectrum: the pediatric ophthalmology perspective
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The COL4A1/COL4A2 ocular phenotypic spectrum: the pediatric ophthalmology perspective

admin2024-08-03T14:48:23+02:0003/08/2024|News, Resources|

Kidney manifestations in COL4A1/COL4A2 related diseases
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Kidney manifestations in COL4A1/COL4A2 related diseases

admin2024-08-03T14:44:11+02:0003/08/2024|News, Resources|

The French COL4A1/COL4A2 cohort: phenotypic spectrum
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The French COL4A1/COL4A2 cohort: phenotypic spectrum

admin2024-08-03T14:40:09+02:0003/08/2024|News, Resources|

Handling genetic cerebral small vessel diseases: care organization in France and collaboration at the European level
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Handling genetic cerebral small vessel diseases: care organization in France and collaboration at the European level

admin2024-10-18T07:19:47+02:0010/07/2024|European Conference, News, Resources|

Neuroimaging aspects: from prenatal to adulthood
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Neuroimaging aspects: from prenatal to adulthood

admin2024-07-10T13:32:41+02:0010/07/2024|European Conference, News, Resources|

Gene therapy for rare genetic vascular disorders: a patient-driven journey in drug development
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Gene therapy for rare genetic vascular disorders: a patient-driven journey in drug development

admin2024-07-10T13:22:13+02:0010/07/2024|European Conference, News, Resources|

Overview of clinical and neuroradiological features of COL4A1/A2 adult patients
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Overview of clinical and neuroradiological features of COL4A1/A2 adult patients

admin2024-07-10T13:10:54+02:0010/07/2024|European Conference, News, Resources|

Establishing foundations for translational interventions
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Establishing foundations for translational interventions

admin2024-06-16T20:19:21+02:0016/06/2024|European Conference, News, Resources|

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Associazione Famiglie COL4A1-A2 APS is a non-profit organization made up of family members of children and adults with the COL4A1 / COL4A2 gene mutation.

If a member of your family has this rare mutation, write us to join.

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