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Livres
Articles (34)
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Hereditary Elliptocytosis: A Rare Red Cell Membrane Disorder

Warang, Prashant, Kedar, Prabhakar

Journal:

Indian Journal of Hematology and Blood Transfusion

Année:

2018

Langue:

english

Fichier:

PDF, 2.04 MB

english, 2018

Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations

Devendra, Rati, Gupta, Vinodkumar, Shanmugam, Rajasubramaniam, Singh, M.P.S.S., Patel, Purushottam, Valecha, Neena, Mishra, Neelima, Ahmed, Naseem, Hoti, S.L., Hegde, Harsha V., Warang, Prashant, Chid

Journal:

Infection, Genetics and Evolution

Année:

2020

Fichier:

PDF, 2.16 MB

2020

Applications of imaging flow cytometry in the diagnostic assessment of red cell membrane disorders

More, Tejashree Anil, Dalal, Bhavik, Devendra, Rati, Warang, Prashant, Shankarkumar, Aruna, Kedar, Prabhakar

Journal:

Cytometry Part B: Clinical Cytometry

Année:

2019

Langue:

english

Fichier:

PDF, 4.18 MB

english, 2019

Mutation Update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia

Gupta, Vinod, Kulkarni, Anuja, Warang, Prashant, Devendra, Rati, Chiddarwar, Ashish, Kedar, Prabhakar

Journal:

Human Mutation

Année:

2020

Langue:

english

Fichier:

PDF, 574 KB

english, 2020

Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D

Boris E. Shmukler, Prabhakar S. Kedar, Prashant Warang, Mukesh Desai, Manisha Madkaikar, Kanjaksha Ghosh, Roshan B. Colah, Seth L. Alper

Journal:

American Journal of Hematology

Année:

2010

Langue:

english

Fichier:

PDF, 1.04 MB

english, 2010

Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: Compound heterozygous for NADH-cytochrome b5 reductase gene mutations

Prabhakar S. Kedar, Prashant Warang, Kanjaksha Ghosh, Roshan B. Colah

Journal:

American Journal of Hematology

Année:

2011

Langue:

english

Fichier:

PDF, 150 KB

english, 2011

Flow cytometric osmotic fragility—An effective screening approach for red cell membranopathies

Prashant Warang, Maya Gupta, Prabhakar Kedar, Kanjaksha Ghosh, Roshan Colah

Journal:

Cytometry Part B: Clinical Cytometry

Année:

2011

Langue:

english

Fichier:

PDF, 679 KB

english, 2011

Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family

Neerja Gupta, Paola Bianchi, Elisa Fermo, Madhulika Kabra, Prashant Warang, Prabhakar Kedar, Nomeeta Gupta, Roshan Colah

Journal:

Prenatal Diagnosis

Année:

2007

Langue:

english

Fichier:

PDF, 86 KB

english, 2007

Red cell pyruvate kinase deficiency in neonatal jaundice cases in India

Prabhakar S. Kedar, Prashant Warang, Roshan B. Colah, Dipika Mohanty

Journal:

Indian Journal of Pediatrics

Année:

2006

Langue:

english

Fichier:

PDF, 346 KB

english, 2006

A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia

Prabhakar S. Kedar, Prashant Warang, Anita H. Nadkarni, Roshan B. Colah, Kanjaksha Ghosh

Journal:

Blood Cells, Molecules, and Diseases

Année:

2008

Langue:

english

Fichier:

PDF, 663 KB

english, 2008

New missense homozygous mutation (Q270Ter) in the pyrimidine 5′ nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia

Prashant Warang, Prabhakar Kedar, Rakhee Kar, Kanjaksha Ghosh…

Journal:

Annals of Hematology

Année:

2013

Langue:

english

Fichier:

PDF, 223 KB

english, 2013

Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family

Prabhakar Kedar, Prashant Warang, Kanjaksha Ghosh, Roshan Colah

Journal:

Annals of Hematology

Année:

2012

Langue:

english

Fichier:

PDF, 130 KB

english, 2012

Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene

Prashant Warang, Prabhakar Kedar, Kanjaksha Ghosh…

Journal:

International Journal of Hematology

Année:

2012

Langue:

english

Fichier:

PDF, 324 KB

english, 2012

Molecular and clinical heterogeneity in pyruvate kinase deficiency in India

Warang, Prashant, Kedar, Prabhakar, Ghosh, Kanjaksha, Colah, Roshan

Journal:

Blood Cells, Molecules, and Diseases

Année:

2013

Langue:

english

Fichier:

PDF, 380 KB

english, 2013

Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?

Warang, Prashant, Devendra, Rati, D’Silva, Selma, Chiddarwar, Ashish, Kedar, Prabhakar, Ghosh, Kanjaksha, Colah, Roshan, Mukherjee, Malay B.

Journal:

Annals of Hematology

Année:

2015

Langue:

english

Fichier:

PDF, 102 KB

english, 2015

Primaquine-induced severe methemoglobinemia developed during treatment of Plasmodium vivax malarial infection in an Indian family associated with a novel mutation (p.Agr57Trp) in the CYB5R3 gene

Kedar, Prabhakar, Warang, Prashant, Sanyal, Subhaprakash, Devendra, Rati, Ghosh, Kanjaksha, Colah, Roshan

Journal:

Clinica Chimica Acta

Année:

2014

Langue:

english

Fichier:

PDF, 648 KB

english, 2014

Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches

Warang, Prashant, Nair, Sona, Nadkarni, Anita, Ghosh, Kanjaksha, Colah, Roshan B.

Journal:

Hemoglobin

Année:

2010

Langue:

english

Fichier:

PDF, 94 KB

english, 2010

Hemoglobinopathy Screening by Osmotic Fragility Test Based on Flow Cytometer or Naked Eye

Mohapatra, Rinkle, Warang, Prashant, Ghosh, Kanjaksha, Colah, Roshan

Journal:

Cytometry Part B: Clinical Cytometry

Année:

2014

Langue:

english

Fichier:

PDF, 1.02 MB

english, 2014

Hemoglobinopathy screening by osmotic fragility test based on flow cytometer or naked eye

Mohapatra, Rinkle, Warang, Prashant, Ghosh, Kanjaksha, Colah, Roshan

Journal:

Cytometry Part B: Clinical Cytometry

Année:

2014

Langue:

english

Fichier:

PDF, 343 KB

english, 2014

Erythrocytosis, methemoglobinemia, and the saturation gap

Koduri, Prasad R., Kedar, Prabhakar S., Warang, Prashant

Journal:

Annals of Hematology

Année:

2015

Langue:

english

Fichier:

PDF, 65 KB

english, 2015

Hb Koln [β98(FG5) [GTG → ATG, Val → Met]: The first report from India

Warang, Prashant, Nair, Sona, Nadkarni, Anita, Kedar, Prabhakar, Bhave, Abhay, Ghosh, Kanjaksha, Colah, Roshan

Journal:

Hematology (Maney Publishing)

Année:

2014

Langue:

english

Fichier:

PDF, 143 KB

english, 2014

Spectrum of red cell abnormalities in undiagnosed hemolytic anemias and methemoglobinemias: a single center experience

Warang, Prashant, Kedar, Prabhakar, Ghosh, Kanjaksha, Colah, Roshan B.

Journal:

Clinical Chemistry and Laboratory Medicine

Année:

2015

Langue:

english

Fichier:

PDF, 445 KB

english, 2015

A novel nine base deletion mutation in NADH-cytochrome b5 reductase gene in an Indian family with recessive congenital methemoglobinemia-type-II

Warang, Prashant, Kedar, Prabhakar, Sivanandam, S., Jothilakshmi, K., Sumathi, R., Colah, Roshan

Journal:

Molecular Genetics and Metabolism Reports

Année:

2015

Langue:

english

Fichier:

PDF, 585 KB

english, 2015

Does novel P5′N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?

Warang, Prashant, Devendra, Rati, Chiddarwar, Ashish, Gupta, Vinod, Mirgal, Darshana, Jadli, Anshul, Mohite, Aniket, Kedar, Prabhakar, Mukherjee, Malay

Journal:

Blood Cells, Molecules, and Diseases

Année:

2017

Langue:

english

Fichier:

PDF, 669 KB

english, 2017

Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations

Kedar, Prabhakar, Parmar, Vaishali, Devendra, Rati, Gupta, Vinod, Warang, Prashant, Madkaikar, Manisha

Journal:

Annals of Hematology

Année:

2017

Langue:

english

Fichier:

PDF, 6.12 MB

english, 2017

Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I

Kedar, Prabhakar S., Gupta, Vinod, Warang, Prashant, Chiddarwar, Ashish, Madkaikar, Manisha

Journal:

Hematology (Maney Publishing)

Année:

2018

Langue:

english

Fichier:

PDF, 1.61 MB

english, 2018

Potential involvement of ubiquitin-proteasome system dysfunction associated with oxidative stress in the pathogenesis of sickle cell disease

Warang, Prashant, Homma, Takujiro, Pandya, Riddhi, Sawant, Anuja, Shinde, Nikhil, Pandey, Debjeet, Fujii, Junichi, Madkaikar, Manisha, Mukherjee, Malay B.

Journal:

British Journal of Haematology

Année:

2018

Langue:

english

Fichier:

PDF, 468 KB

english, 2018

Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients

Kedar, Prabhakar S, Gupta, Vinod, Dongerdiye, Rashmi, Chiddarwar, Ashish, Warang, Prashant, Madkaikar, Manisha R

Journal:

Journal of Clinical Pathology

Année:

2018

Langue:

english

Fichier:

PDF, 455 KB

english, 2018

Red cell adenylate kinase deficiency in India: identification of two novel missense mutations (c.71A>G and c.413G>A)

Dongerdiye, Rashmi, Kamat, Pranoti, Jain, Punit, Warang, Prashant, Devendra, Rati, Wasekar, Nilesh, Sharma, Ratna, Mhaskar, Ketaki, Madkaikar, Manisha R, Manglani, Mamta V, Kedar, Prabhakar S

Journal:

Journal of Clinical Pathology

Année:

2019

Langue:

english

Fichier:

PDF, 1.25 MB

english, 2019

Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction

Kedar, Prabhakar S., Dongerdiye, Rashmi, Chilwirwar, Pooja, Gupta, Vinod, Chiddarwar, Ashish, Devendra, Rati, Warang, Prashant, Prasada, Harsha, Sampagar, Abhilasha, Bhat, Sunil, Chandrakala, S., Madk

Journal:

Indian Journal of Pediatrics

Année:

2019

Langue:

english

Fichier:

PDF, 2.99 MB

english, 2019

Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach

Kedar, Prabhakar S., Harigae, Hideo, Ito, Etsuro, Muramatsu, Hideki, Kojima, Seiji, Okuno, Yusuke, Fujiwara, Tohru, Dongerdiye, Rashmi, Warang, Prashant P., Madkaikar, Manisha R.

Journal:

International Journal of Hematology

Année:

2019

Langue:

english

Fichier:

PDF, 566 KB

english, 2019

Mutation Update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia

Gupta, Vinod, Kulkarni, Anuja, Warang, Prashant, Devendra, Rati, Chiddarwar, Ashish, Kedar, Prabhakar

Journal:

Human Mutation

Année:

2020

Fichier:

PDF, 574 KB

2020

Lead Poisoning Induced Severe Hemolytic Anemia, Basophilic Stippling, Mimicking Erythrocyte Pyrimidine 5'-nucleotidase Deficiency in Beta Thalassemia Minor

Warang, Prashant, Colah, Roshan, Kedar, Prabhakar

Journal:

Journal of Clinical Toxicology

Année:

2017

Fichier:

PDF, 551 KB

2017

Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India

More, Tejashree Anil, Dongerdiye, Rashmi, Devendra, Rati, Warang, Prashant P., Kedar, Prabhakar S.

Journal:

Annals of Hematology

Année:

2020

Langue:

english

Fichier:

PDF, 1.09 MB

english, 2020