Author/Creator: Savoia, A. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Savoia, A.

1. Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases. (28th October 2017)

Authors:: Zaninetti, C.; Santini, V.; Tiniakou, M.; Barozzi, S.; Savoia, A.; Pecci, A.
Journal:: Journal of thrombosis and haemostasis
Issue:: Volume 15:Number 12(2017)
Page Start:: 2388
Record Type:: Journal Article
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2. Inherited thrombocytopenias frequently diagnosed in adults. Issue 6 (3rd July 2013)

Authors:: Balduini, C. L.; Savoia, A.; Seri, M.
Journal:: Journal of thrombosis and haemostasis
Issue:: Volume 11:Issue 6(2013)
Page Start:: 1006
Record Type:: Journal Article
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3. Molecular basis of inherited thrombocytopenias. Issue 2 (28th May 2015)

Authors:: Savoia, A.
Journal:: Clinical genetics
Issue:: Volume 89:Issue 2(2016)
Page Start:: 154
Record Type:: Journal Article
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4. Molecular diagnosis of thrombocytopenia‐absent radius syndrome using next‐generation sequencing. (20th June 2016)

Authors:: Nicchia, E.; Giordano, P.; Greco, C.; De Rocco, D.; Savoia, A.
Journal:: International journal of laboratory hematology
Issue:: Volume 38:Number 4(2016:Aug.)
Page Start:: 412
Record Type:: Journal Article
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5. R705H mutation of MYH9 is associated with MYH9‐related disease and not only with non‐syndromic deafness DFNA17. (26th July 2014)

Authors:: Verver, E.; Pecci, A.; De Rocco, D.; Ryhänen, S.; Barozzi, S.; Kunst, H.; Topsakal, V.; Savoia, A.
Journal:: Clinical genetics
Issue:: Volume 88:Number 1(2015:Jul.)
Page Start:: 85
Record Type:: Journal Article
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