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Valentina Lanari
Valentina Lanari
Boston Children's Hospital
Phenotype
Mutation
Endocrinology
Exome sequencing
Cortical dysplasia
2
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5
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0
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TUBB3 E410K syndrome: Case report and review of the clinical spectrum of TUBB3 mutations.
2020
American Journal of Medical Genetics Part A
Maria Lisa Dentici
Vittorio Maglione
Emanuele Agolini
Gino Catena
Rossella Capolino
Valentina Lanari
Antonio Novelli
Lorenzo Sinibaldi
Davide Vecchio
Michaela Veronika Gonfiantini
Marina Macchiaiolo
Maria Cristina Digilio
Bruno Dallapiccola
Andrea Bartuli
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Citations (3)
IFNAR2 Deficiency Causing Dysregulation of NK Cell Functions and Presenting With Hemophagocytic Lymphohistiocytosis
2020
Frontiers in Genetics
Chiara Passarelli
Adele Civino
Marianna N. Rossi
Loredana Cifaldi
Valentina Lanari
Gian Marco Moneta
Ivan Caiello
Claudia Bracaglia
Raffaele Montinaro
Antonio Novelli
Fabrizio De Benedetti
Giusi Prencipe
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Citations (2)
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