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Nature Genetics
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October 16, 2012
Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma
Elizabeth Pohler, Ons Mamai, Jennifer Hirst, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 24, 2017
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
Ahmed Khattab, Shozeb Haider, Ameet Kumar, et al.
Nature Genetics
|
June 1, 2010
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes
Enza Maria Valente, Clare V Logan, Soumaya Mougou-Zerelli, et al.
Frontiers in Medicine
|
August 4, 2022
Development and implementation of the AIDA international registry for patients with Schnitzler's syndrome
Jurgen Sota, Antonio Vitale, Ewa Więsik-Szewczyk, et al.
Frontiers in Medicine
|
June 27, 2022
Development and Implementation of the AIDA International Registry for Patients With Undifferentiated Systemic AutoInflammatory Diseases
Francesca Della Casa, Antonio Vitale, Giuseppe Lopalco, et al.
Rheumatology (Oxford, England)
|
April 2, 2025
Predictors of proteinuria, amyloidosis and kidney failure in familial Mediterranean fever: data from the International AIDA Network Registry
Antonio Vitale, Valeria Caggiano, Jessica Sbalchiero, et al.
Frontiers in Immunology
|
May 27, 2024
Risk for cancer development in familial Mediterranean fever and associated predisposing factors: an ambidirectional cohort study from the international AIDA Network registries
Antonio Vitale, Valeria Caggiano, Abdurrahman Tufan, et al.
Internal and Emergency Medicine
|
December 27, 2023
Correction: Clinical and laboratory features associated with macrophage activation syndrome in Still's disease: data from the international AIDA Network Still's Disease Registry
Paola Triggianese, Antonio Vitale, Giuseppe Lopalco, et al.
Internal and Emergency Medicine
|
October 12, 2023
Clinical and laboratory features associated with macrophage activation syndrome in Still's disease: data from the international AIDA Network Still's Disease Registry
Paola Triggianese, Antonio Vitale, Giuseppe Lopalco, et al.
Rheumatology (Oxford, England)
|
November 19, 2025
Risk of major organ involvement in Behçet's patients with mucocutaneous onset: data from the AIDA Network Registry
Antonio Vitale, Francesco Gavioli, Valeria Caggiano, et al.
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of 37
Search research articles
Search
Showing results (351-360 of 361) with videos related to
Sort By:
Page
of 37
Nature Genetics
|
October 16, 2012
Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma
Elizabeth Pohler, Ons Mamai, Jennifer Hirst, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 24, 2017
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
Ahmed Khattab, Shozeb Haider, Ameet Kumar, et al.
Nature Genetics
|
June 1, 2010
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes
Enza Maria Valente, Clare V Logan, Soumaya Mougou-Zerelli, et al.
Frontiers in Medicine
|
August 4, 2022
Development and implementation of the AIDA international registry for patients with Schnitzler's syndrome
Jurgen Sota, Antonio Vitale, Ewa Więsik-Szewczyk, et al.
Frontiers in Medicine
|
June 27, 2022
Development and Implementation of the AIDA International Registry for Patients With Undifferentiated Systemic AutoInflammatory Diseases
Francesca Della Casa, Antonio Vitale, Giuseppe Lopalco, et al.
Rheumatology (Oxford, England)
|
April 2, 2025
Predictors of proteinuria, amyloidosis and kidney failure in familial Mediterranean fever: data from the International AIDA Network Registry
Antonio Vitale, Valeria Caggiano, Jessica Sbalchiero, et al.
Frontiers in Immunology
|
May 27, 2024
Risk for cancer development in familial Mediterranean fever and associated predisposing factors: an ambidirectional cohort study from the international AIDA Network registries
Antonio Vitale, Valeria Caggiano, Abdurrahman Tufan, et al.
Internal and Emergency Medicine
|
December 27, 2023
Correction: Clinical and laboratory features associated with macrophage activation syndrome in Still's disease: data from the international AIDA Network Still's Disease Registry
Paola Triggianese, Antonio Vitale, Giuseppe Lopalco, et al.
Internal and Emergency Medicine
|
October 12, 2023
Clinical and laboratory features associated with macrophage activation syndrome in Still's disease: data from the international AIDA Network Still's Disease Registry
Paola Triggianese, Antonio Vitale, Giuseppe Lopalco, et al.
Rheumatology (Oxford, England)
|
November 19, 2025
Risk of major organ involvement in Behçet's patients with mucocutaneous onset: data from the AIDA Network Registry
Antonio Vitale, Francesco Gavioli, Valeria Caggiano, et al.
Page
of 37