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Pipeline embolization of posterior circulation aneurysms: a multicenter study of 131 aneurysms

Journal of neurosurgery, 2019-03, Vol.130 (3), p.923-935

2019

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Alport syndrome: impact of digenic inheritance in patients management

Clinical genetics, 2017-07, Vol.92 (1), p.34-44

2017

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Posterior Circulation Endovascular Thrombectomy for Large-Vessel Occlusion: Predictors of Favorable Clinical Outcome and Analysis of First-Pass Effect

American journal of neuroradiology : AJNR, 2021-05, Vol.42 (5), p.896-903

2021

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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

Science (American Association for the Advancement of Science), 2020-10, Vol.370 (6515)

2020

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Non-collagen genes role in digenic Alport syndrome

BMC nephrology, 2019-02, Vol.20 (1), p.70-70, Article 70

2019

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Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B

Clinical genetics, 2012-09, Vol.82 (3), p.248-255

2012

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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Nature (London), 2011-10, Vol.478 (7367), p.97-102

2011

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X-linked Alport syndrome: Natural history and genotype-phenotype correlations in girls and women belonging to 195 families: A European Community Alport Syndrome Concerted Action Study

Journal of the American Society of Nephrology, 2003-10, Vol.14 (10), p.2603-2610

2003

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Autosomal-dominant Alport syndrome: Natural history of a disease due to COL4A3 or COL4A4 gene

Kidney international, 2004-05, Vol.65 (5), p.1598-1603

2004

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International Study of Intracranial Aneurysm Treatment Using Woven EndoBridge: Results of the WorldWideWEB Consortium

Stroke (1970), 2022-02, Vol.53 (2), p.e47-e49

2022

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Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes

Molecular psychiatry, 2017-06, Vol.22 (6), p.836-849

2017

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Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality

The Journal of clinical investigation, 2021-12, Vol.131 (23)

2021

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Association between primary open-angle glaucoma (POAG) and WDR36 sequence variance in Italian families affected by POAG

British journal of ophthalmology, 2011-05, Vol.95 (5), p.624-626

2011

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Mechanical thrombectomy beyond the circle of Willis: efficacy and safety of different techniques for M2 occlusions

Journal of neurointerventional surgery, 2022-06, Vol.14 (6), p.546

2022

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The Woven EndoBridge (WEB) Device for the Treatment of Intracranial Aneurysms: Ten Years of Lessons Learned and Adjustments in Practice from the WorldWideWEB Consortium

Translational stroke research, 2023-08, Vol.14 (4), p.455-464

2023

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Effects of Hyper-Early (<12 Hours) Endovascular Treatment of Ruptured Intracranial Aneurysms on Clinical Outcome

Interventional neuroradiology, 2013-06, Vol.19 (2), p.195-202

2013

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Comparison of PED and FRED flow diverters for posterior circulation aneurysms: a propensity score matched cohort study

Journal of neurointerventional surgery, 2021-02, Vol.13 (2), p.153

2021

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Chronic eyelid oedema and rosacea (Morbus Morbihan): diagnostic and therapeutic challenges

Klinische Monatsblatter fur Augenheilkunde, 2011-01, Vol.228 (1), p.19

2011

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Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families

Nephrology, dialysis, transplantation, 2006-03, Vol.21 (3), p.665-671

2006

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Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis—a collaborative study of the Italian Renal Immunopathology Group

Nephrology, dialysis, transplantation, 2005-03, Vol.20 (3), p.545-551

2005

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Vav1 Haploinsufficiency in a Common Variable Immunodeficiency Patient with Defective T-Cell Function

International journal of immunopathology and pharmacology, 2012-07, Vol.25 (3), p.811-817

2012

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The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP

Orphanet journal of rare diseases, 2013-04, Vol.8 (1), p.63-63

2013

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A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure

Human reproduction (Oxford), 2009-08, Vol.24 (8), p.2023-2028

2009

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Epidermal basement membrane alpha 5(IV) expression in females with Alport syndrome and severity of renal disease

Kidney international, 2003-11, Vol.64 (5), p.1787-1791

2003

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Pipeline embolization of posterior circulation aneurysms: a multicenter study of 131 aneurysms

Alport syndrome: impact of digenic inheritance in patients management

Posterior Circulation Endovascular Thrombectomy for Large-Vessel Occlusion: Predictors of Favorable Clinical Outcome and Analysis of First-Pass Effect

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

Non-collagen genes role in digenic Alport syndrome

Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

X-linked Alport syndrome: Natural history and genotype-phenotype correlations in girls and women belonging to 195 families: A European Community Alport Syndrome Concerted Action Study

Autosomal-dominant Alport syndrome: Natural history of a disease due to COL4A3 or COL4A4 gene

International Study of Intracranial Aneurysm Treatment Using Woven EndoBridge: Results of the WorldWideWEB Consortium

Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes

Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality

Association between primary open-angle glaucoma (POAG) and WDR36 sequence variance in Italian families affected by POAG

Mechanical thrombectomy beyond the circle of Willis: efficacy and safety of different techniques for M2 occlusions

The Woven EndoBridge (WEB) Device for the Treatment of Intracranial Aneurysms: Ten Years of Lessons Learned and Adjustments in Practice from the WorldWideWEB Consortium

Effects of Hyper-Early (<12 Hours) Endovascular Treatment of Ruptured Intracranial Aneurysms on Clinical Outcome

Comparison of PED and FRED flow diverters for posterior circulation aneurysms: a propensity score matched cohort study

Chronic eyelid oedema and rosacea (Morbus Morbihan): diagnostic and therapeutic challenges

Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families

Effect of extracranial lesion severity on outcome of endovascular thrombectomy in patients with anterior circulation tandem occlusion: analysis of the TITAN registry

Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis—a collaborative study of the Italian Renal Immunopathology Group

Vav1 Haploinsufficiency in a Common Variable Immunodeficiency Patient with Defective T-Cell Function

The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP

A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure

Epidermal basement membrane alpha 5(IV) expression in females with Alport syndrome and severity of renal disease

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