Contact us   |  

Members

Information

Bianchi, Paola

About me

Name: Paola

Surname: Bianchi

Academic title: BSc, PhD

Charge: Head Biologist


Which is your area of expertise for the "Disease/group of diseases"?

  • Diagnostics

Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):

Red cell disorders, hemolytic anemias, disesrytropoietic anemias , Diagnosis, Molecular diagnosis

Diseases:

Thrombocytopenia with congenital dyserythropoietic anemia X-linked dyserythropoetic anemia with abnormal platelets and neutropenia Rare anemia Rare hemolytic anemia Rare constitutional hemolytic anemia Lethal hemolytic anemia-genital anomalies syndrome Atypical hemolytic-uremic syndrome Atypical hemolytic-uremic syndrome with DGKE deficiency Atypical hemolytic-uremic syndrome with C3 anomaly Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly Atypical hemolytic-uremic syndrome with B factor anomaly Atypical hemolytic-uremic syndrome with H factor anomaly Atypical hemolytic-uremic syndrome with I factor anomaly Atypical hemolytic-uremic syndrome with anti-factor H antibodies Atypical hemolytic-uremic syndrome with thrombomodulin anomaly Familial LCAT deficiency Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome Rare constitutional hemolytic anemia due to a red cell membrane anomaly Hereditary spherocytosis Hereditary elliptocytosis Distal renal tubular acidosis with anemia Hereditary stomatocytosis Overhydrated hereditary stomatocytosis Dehydrated hereditary stomatocytosis Rh deficiency syndrome Familial pseudohyperkalemia Southeast Asian ovalocytosis Hereditary cryohydrocytosis with reduced stomatin Hereditary cryohydrocytosis with normal stomatin Constitutional hemolytic anemia due to acanthocytosis Abetalipoproteinemia McLeod neuroacanthocytosis syndrome Primary CD59 deficiency Rare constitutional hemolytic anemia due to an enzyme disorder Congenital erythropoietic porphyria Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies Glutathione synthetase deficiency Glutathione synthetase deficiency with 5-oxoprolinuria Glutathione synthetase deficiency without 5-oxoprolinuria Gamma-glutamylcysteine synthetase deficiency Hemolytic anemia due to glutathione reductase deficiency 6-phosphogluconate dehydrogenase deficiency Hemolytic anemia due to a disorder of glycolytic enzymes Glycogen storage disease due to muscle phosphofructokinase deficiency Triose phosphate-isomerase deficiency Glycogen storage disease due to aldolase A deficiency Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Hemolytic anemia due to red cell pyruvate kinase deficiency Hemolytic anemia due to glucophosphate isomerase deficiency Hemolytic anemia due to diphosphoglycerate mutase deficiency Non-spherocytic hemolytic anemia due to hexokinase deficiency Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Class I glucose-6-phosphate dehydrogenase deficiency Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency Hemolytic anemia due to adenylate kinase deficiency Hemolytic anemia due to erythrocyte adenosine deaminase overproduction Heinz body anemia Constitutional dyserythropoietic anemia Congenital dyserythropoietic anemia Congenital dyserythropoietic anemia type I Congenital dyserythropoietic anemia type III Congenital dyserythropoietic anemia type II Congenital dyserythropoietic anemia type IV

Which is your patient age coverage?

  • Pediatrics
  • Adults


Member Go to member

Name english: Foundation IRCCS Ca’Granda Ospedale Maggiore Policlinico, Milan

Name original: Fondazione IRCCS CA'Granda Ospedale Maggiore Policlinico , Milano


Healthcare provider Go to healthcare provider

Name english: Foundation IRCCS Ca’Granda Ospedale Maggiore Policlinico, Milan

Name original: Fondazione IRCCS CA'Granda Ospedale Maggiore Policlinico , Milano

Departments

English name Original name Subnetworks of expertise Healthcare provider