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Indian Journal of Pediatrics
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April 19, 2016
Adenosine Deaminase Deficiency with a Novel Gene Mutation
Maya Gupta, Jahnavi Aluri, Antony Terrance, et al.
European Journal of Haematology
|
August 19, 2009
Paroxysmal nocturnal haemoglobinuria: diagnostic tests, advantages, & limitations
Manisha Madkaikar, Maya Gupta, Farah Jijina, et al.
Journal of Pediatric Hematology/Oncology
|
June 9, 2016
Predominant Neurologic Manifestations Seen in a Patient With a Biallelic Perforin1 Mutation (PRF1; p.R225W)
Manisha Madkaikar, Maya Gupta, Ashish Dixit, et al.
Journal of Theoretical Biology
|
September 20, 2021
Understanding memory B cell selection
Stephen Lindsly, Maya Gupta, Cooper Stansbury, et al.
Expert Review of Neurotherapeutics
|
July 1, 2014
Measuring negative symptom change in schizophrenia: considering alternatives to self-report
Maya Gupta, Katherine Holshausen, Lisa Gou, et al.
European Journal of Haematology
|
March 31, 2011
Advances in autoimmune lymphoproliferative syndromes
Manisha Madkaikar, Snehal Mhatre, Maya Gupta, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology
|
January 4, 2014
Evaluation of danazol, cyclosporine, and prednisolone as single agent or in combination for paroxysmal nocturnal hemoglobinuria
Kanjaksha Ghosh, Manisha Madkaikar, Maya Gupta, et al.
Indian Journal of Pediatrics
|
April 6, 2012
Prenatal diagnosis of LAD-I on cord blood by flowcytometry
Manisha Rajan Madkaikar, Maya Gupta, Meghana Rao, et al.
Journal of Psychiatric Research
|
September 28, 2011
Functional outcomes in schizophrenia: understanding the competence-performance discrepancy
Maya Gupta, Emma Bassett, Felicia Iftene, et al.
Journal of Clinical Immunology
|
February 19, 2014
Rapid Flow cytometric prenatal diagnosis of primary immunodeficiency (PID) disorders
Anju Mishra, Maya Gupta, Aparna Dalvi, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 74) with videos related to
Sort By:
Page
of 8
Indian Journal of Pediatrics
|
April 19, 2016
Adenosine Deaminase Deficiency with a Novel Gene Mutation
Maya Gupta, Jahnavi Aluri, Antony Terrance, et al.
European Journal of Haematology
|
August 19, 2009
Paroxysmal nocturnal haemoglobinuria: diagnostic tests, advantages, & limitations
Manisha Madkaikar, Maya Gupta, Farah Jijina, et al.
Journal of Pediatric Hematology/Oncology
|
June 9, 2016
Predominant Neurologic Manifestations Seen in a Patient With a Biallelic Perforin1 Mutation (PRF1; p.R225W)
Manisha Madkaikar, Maya Gupta, Ashish Dixit, et al.
Journal of Theoretical Biology
|
September 20, 2021
Understanding memory B cell selection
Stephen Lindsly, Maya Gupta, Cooper Stansbury, et al.
Expert Review of Neurotherapeutics
|
July 1, 2014
Measuring negative symptom change in schizophrenia: considering alternatives to self-report
Maya Gupta, Katherine Holshausen, Lisa Gou, et al.
European Journal of Haematology
|
March 31, 2011
Advances in autoimmune lymphoproliferative syndromes
Manisha Madkaikar, Snehal Mhatre, Maya Gupta, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology
|
January 4, 2014
Evaluation of danazol, cyclosporine, and prednisolone as single agent or in combination for paroxysmal nocturnal hemoglobinuria
Kanjaksha Ghosh, Manisha Madkaikar, Maya Gupta, et al.
Indian Journal of Pediatrics
|
April 6, 2012
Prenatal diagnosis of LAD-I on cord blood by flowcytometry
Manisha Rajan Madkaikar, Maya Gupta, Meghana Rao, et al.
Journal of Psychiatric Research
|
September 28, 2011
Functional outcomes in schizophrenia: understanding the competence-performance discrepancy
Maya Gupta, Emma Bassett, Felicia Iftene, et al.
Journal of Clinical Immunology
|
February 19, 2014
Rapid Flow cytometric prenatal diagnosis of primary immunodeficiency (PID) disorders
Anju Mishra, Maya Gupta, Aparna Dalvi, et al.
Page
of 8