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Indian Pediatrics
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May 21, 2021
Pediatric Hemophagocytic Lymphohistiocytosis - A Single Center Study
Tanusree Paul, Manas Kalra, Arun Danewa, et al.
The Indian Journal of Medical Research
|
June 6, 2022
High soluble interleukin-2 receptor values in Indian paediatric & adult controls - Need for population-specific threshold in the diagnosis of haemophagocytic lymphohistiocytosis
Veronique Dinand, Anupam Sachdeva, Sakshi Sharma, et al.
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi
|
March 4, 2014
Threshold of galactomannan antigenemia positivity for early diagnosis of invasive aspergillosis in neutropenic children
Veronique Dinand, Madasu Anjan, Jaswinder Kaur Oberoi, et al.
Pediatric Hematology and Oncology
|
January 4, 2014
Hemophagocytic lymphohistiocytosis in infants: a single center experience from India
Mohammed Ramzan, Satya Prakash Yadav, Gaurav Kharya, et al.
Pediatric Blood & Cancer
|
June 11, 2010
Langerhans cell histiocytosis with digestive tract involvement
Satya P Yadav, Gaurav Kharya, Neelam Mohan, et al.
Indian Journal of Pediatrics
|
November 29, 2012
Antioxidant levels at diagnosis in childhood acute lymphoblastic leukemia
Nita Radhakrishnan, Veronique Dinand, Spriha Rao, et al.
Journal of Pediatric Hematology/Oncology
|
November 20, 2010
Human heme oxygenase-1 deficiency presenting with hemolysis, nephritis, and asplenia
Nita Radhakrishnan, Satya Prakash Yadav, Anupam Sachdeva, et al.
Indian Pediatrics
|
April 8, 2019
Consensus Statement of the Indian Academy of Pediatrics on Diagnosis and Management of Fragile X Syndrome in India
Anupam Sachdeva, Prachi Jain, Vinod Gunasekaran, et al.
Indian Pediatrics
|
July 7, 2018
Umbilical Cord Blood Banking: Consensus Statement of the Indian Academy of Pediatrics
Anupam Sachdeva, Vinod Gunasekaran, Payal Malhotra, et al.
Hematology/Oncology and Stem Cell Therapy
|
December 17, 2013
Severe combined immunodeficiency caused by a new homozygous RAG1 mutation with progressive encephalopathy
Nivedita Dhingra, Satya Prakash Yadav, Jean-Pierre de Villartay, et al.
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of 10
Search research articles
Search
Showing results (71-80 of 91) with videos related to
Sort By:
Page
of 10
Indian Pediatrics
|
May 21, 2021
Pediatric Hemophagocytic Lymphohistiocytosis - A Single Center Study
Tanusree Paul, Manas Kalra, Arun Danewa, et al.
The Indian Journal of Medical Research
|
June 6, 2022
High soluble interleukin-2 receptor values in Indian paediatric & adult controls - Need for population-specific threshold in the diagnosis of haemophagocytic lymphohistiocytosis
Veronique Dinand, Anupam Sachdeva, Sakshi Sharma, et al.
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi
|
March 4, 2014
Threshold of galactomannan antigenemia positivity for early diagnosis of invasive aspergillosis in neutropenic children
Veronique Dinand, Madasu Anjan, Jaswinder Kaur Oberoi, et al.
Pediatric Hematology and Oncology
|
January 4, 2014
Hemophagocytic lymphohistiocytosis in infants: a single center experience from India
Mohammed Ramzan, Satya Prakash Yadav, Gaurav Kharya, et al.
Pediatric Blood & Cancer
|
June 11, 2010
Langerhans cell histiocytosis with digestive tract involvement
Satya P Yadav, Gaurav Kharya, Neelam Mohan, et al.
Indian Journal of Pediatrics
|
November 29, 2012
Antioxidant levels at diagnosis in childhood acute lymphoblastic leukemia
Nita Radhakrishnan, Veronique Dinand, Spriha Rao, et al.
Journal of Pediatric Hematology/Oncology
|
November 20, 2010
Human heme oxygenase-1 deficiency presenting with hemolysis, nephritis, and asplenia
Nita Radhakrishnan, Satya Prakash Yadav, Anupam Sachdeva, et al.
Indian Pediatrics
|
April 8, 2019
Consensus Statement of the Indian Academy of Pediatrics on Diagnosis and Management of Fragile X Syndrome in India
Anupam Sachdeva, Prachi Jain, Vinod Gunasekaran, et al.
Indian Pediatrics
|
July 7, 2018
Umbilical Cord Blood Banking: Consensus Statement of the Indian Academy of Pediatrics
Anupam Sachdeva, Vinod Gunasekaran, Payal Malhotra, et al.
Hematology/Oncology and Stem Cell Therapy
|
December 17, 2013
Severe combined immunodeficiency caused by a new homozygous RAG1 mutation with progressive encephalopathy
Nivedita Dhingra, Satya Prakash Yadav, Jean-Pierre de Villartay, et al.
Page
of 10