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Anu Aggarwal

Showing results (11-20 of 45) with videos related to

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Canadian Respiratory Journal|June 14, 2013
An unusual cause of transient ischemic attackMatthew J Brooks, Liam Michael Hannan, AiVee Ng, et al.
Blood Cells, Molecules & Diseases|December 23, 2019
Phenotypic and genetic heterogeneity arising from a novel substitution at amino acid position Val205 in GATA1 related X-linked thrombocytopenia with dyserythropoietic anemiaManu Jamwal, Anu Aggarwal, Prashant Sharma, et al.
Indian Journal of Pediatrics|November 27, 2002
Pelvic ultrasonography in pubertal girlsAnju Seth, Anu Aggarwal, K Sandesh, et al.
JACC. Basic to Translational Science|February 7, 2022
Sex-Dependent Effect of Platelet Nitric Oxide: Production and Platelet Reactivity in Healthy IndividualsMatthew D Godwin, Anu Aggarwal, Zachary Hilt, et al.
Pathology|November 24, 2018
First report of homocystinuria-megaloblastic anaemia, cobalamin E complementation type, in an Indian childManu Jamwal, Anu Aggarwal, Prashant Sharma, et al.
British Journal of Haematology|May 24, 2019
A nonsense variant in the Hexokinase 1 gene (HK1) causing severe non-spherocytic haemolytic anaemia: genetic analysis exemplifies ambiguity due to multiple IsoformsManu Jamwal, Anu Aggarwal, Arindam Palodi, et al.
British Journal of Haematology|October 12, 2019
Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian studyAnu Aggarwal, Manu Jamwal, Prashant Sharma, et al.
Journal of Clinical Pathology|March 22, 2018
Overhydrated stomatocytosis associated with a complex <i>RHAG</i> genotype including a novel <i>de novo</i> mutationManu Jamwal, Anu Aggarwal, Man Updesh Singh Sachdeva, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 25, 2016
Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three casesManu Jamwal, Anu Aggarwal, Verinder Kumar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 23, 2017
Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infantManu Jamwal, Anu Aggarwal, Anirban Das, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Canadian Respiratory Journal|June 14, 2013
An unusual cause of transient ischemic attackMatthew J Brooks, Liam Michael Hannan, AiVee Ng, et al.
Blood Cells, Molecules & Diseases|December 23, 2019
Phenotypic and genetic heterogeneity arising from a novel substitution at amino acid position Val205 in GATA1 related X-linked thrombocytopenia with dyserythropoietic anemiaManu Jamwal, Anu Aggarwal, Prashant Sharma, et al.
Indian Journal of Pediatrics|November 27, 2002
Pelvic ultrasonography in pubertal girlsAnju Seth, Anu Aggarwal, K Sandesh, et al.
JACC. Basic to Translational Science|February 7, 2022
Sex-Dependent Effect of Platelet Nitric Oxide: Production and Platelet Reactivity in Healthy IndividualsMatthew D Godwin, Anu Aggarwal, Zachary Hilt, et al.
Pathology|November 24, 2018
First report of homocystinuria-megaloblastic anaemia, cobalamin E complementation type, in an Indian childManu Jamwal, Anu Aggarwal, Prashant Sharma, et al.
British Journal of Haematology|May 24, 2019
A nonsense variant in the Hexokinase 1 gene (HK1) causing severe non-spherocytic haemolytic anaemia: genetic analysis exemplifies ambiguity due to multiple IsoformsManu Jamwal, Anu Aggarwal, Arindam Palodi, et al.
British Journal of Haematology|October 12, 2019
Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian studyAnu Aggarwal, Manu Jamwal, Prashant Sharma, et al.
Journal of Clinical Pathology|March 22, 2018
Overhydrated stomatocytosis associated with a complex <i>RHAG</i> genotype including a novel <i>de novo</i> mutationManu Jamwal, Anu Aggarwal, Man Updesh Singh Sachdeva, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 25, 2016
Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three casesManu Jamwal, Anu Aggarwal, Verinder Kumar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 23, 2017
Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infantManu Jamwal, Anu Aggarwal, Anirban Das, et al.
Pageof 5