Prabhakar S. Kedar: search on Z-Library

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1

Hereditary Elliptocytosis: A Rare Red Cell Membrane Disorder

Warang, Prashant, Kedar, Prabhakar

Journal:

Indian Journal of Hematology and Blood Transfusion

Year:

2018

Language:

english

File:

PDF, 2.04 MB

english, 2018

2

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

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

Journal:

Year:

2020

Language:

english

File:

PDF, 574 KB

english, 2020

3

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

Year:

2019

Language:

english

File:

PDF, 4.18 MB

english, 2019

4

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

Year:

2011

Language:

english

File:

PDF, 679 KB

english, 2011

5

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

Year:

2017

Language:

english

File:

PDF, 6.12 MB

english, 2017

6

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)

Year:

2018

Language:

english

File:

PDF, 1.61 MB

english, 2018

7

Mapping Direct Observations From Objective Structured Clinical Examinations to the Milestones Across Specialties

Baker-Genaw, Kimberly, Kokas, Maria S., Ahsan, Syed F., Darnley-Fisch, Deborah, Drake, Sean, Goyal, Nikhil, Inamdar, Kedar, Moutzouros, Vasilios, Prabhakar, Deepak, Rolland, Laurie, Sangha, Roopina, S

Journal:

Journal of Graduate Medical Education

Year:

2016

Language:

english

File:

PDF, 119 KB

english, 2016

8

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

Year:

2011

Language:

english

File:

PDF, 150 KB

english, 2011

9

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

Year:

2013

Language:

english

File:

PDF, 223 KB

english, 2013

10

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

Year:

2006

Language:

english

File:

PDF, 346 KB

english, 2006

11

Hereditary spherocytosis in association with severe G6PD deficiency: report of an unusual case

Prabhakar S Kedar, Roshan B Colah, Kanjaksha Ghosh, Dipika Mohanty

Journal:

Clinica Chimica Acta

Year:

2004

Language:

english

File:

PDF, 116 KB

english, 2004

12

Accurate multipixel phase measurement with classical-light interferometry

Singh, Mandeep, Khare, Kedar, Jha, Anand Kumar, Prabhakar, Shashi, Singh, R. P.

Journal:

Physical Review A

Year:

2015

Language:

english

File:

PDF, 1.97 MB

english, 2015

13

Congenital methemoglobinemia caused by Hb-MRatnagiri (β-63CAT→TAT, His→Tyr) in an Indian family

Prabhakar S. Kedar, Anita H. Nadkarni, Supriya Phanasgoankar, Manisha Madkaikar, Kanjaksha Ghosh, Ajit C. Gorakshakar, Roshan B. Colah, Dipika Mohanty

Journal:

American Journal of Hematology

Year:

2005

Language:

english

File:

PDF, 68 KB

english, 2005

14

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)

Year:

2014

Language:

english

File:

PDF, 143 KB

english, 2014

15

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

Year:

2008

Language:

english

File:

PDF, 663 KB

english, 2008

16

Erythrocytosis, methemoglobinemia, and the saturation gap

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

Journal:

Annals of Hematology

Year:

2015

Language:

english

File:

PDF, 65 KB

english, 2015

17

Genotypic analysis of SLC4A1 A858D mutation in Indian population associated with distal renal tubular Acidosis (dRTA) coupled with hemolytic anemia

More, Tejashree Anil, Kedar, Prabhakar S.

Journal:

Year:

2020

File:

PDF, 2.53 MB

2020

18

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

Year:

2015

Language:

english

File:

PDF, 445 KB

english, 2015

19

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

Year:

2010

Language:

english

File:

PDF, 1.04 MB

english, 2010

20

Proteomic investigation on the pyk-F gene knockout Escherichia coli for aromatic amino acid production

Prabhakar Kedar, Roshan Colah, Kazuyuki Shimizu

Journal:

Enzyme and Microbial Technology

Year:

2007

Language:

english

File:

PDF, 1.07 MB

english, 2007

21

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

Year:

2017

Language:

english

File:

PDF, 669 KB

english, 2017

22

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

Year:

2012

Language:

english

File:

PDF, 324 KB

english, 2012

23

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

Year:

2015

Language:

english

File:

PDF, 102 KB

english, 2015

24

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

Year:

2019

Language:

english

File:

PDF, 2.99 MB

english, 2019

25

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

Year:

2019

Language:

english

File:

PDF, 1.25 MB

english, 2019

26

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

Year:

2019

Language:

english

File:

PDF, 566 KB

english, 2019

27

Molecular and clinical heterogeneity in pyruvate kinase deficiency in India

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

Journal:

Blood Cells, Molecules, and Diseases

Year:

2013

Language:

english

File:

PDF, 380 KB

english, 2013

28

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

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

Journal:

Year:

2020

File:

PDF, 574 KB

2020

29

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

Year:

2007

Language:

english

File:

PDF, 86 KB

english, 2007

30

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

Year:

2012

Language:

english

File:

PDF, 130 KB

english, 2012

31

Primary hydatid cyst of neck muscles

Kedar Nath, Girish Prabhakar, R. C. Nagar

Journal:

Indian Journal of Pediatrics

Year:

2002

Language:

english

File:

PDF, 264 KB

english, 2002

32

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

Year:

2014

Language:

english

File:

PDF, 648 KB

english, 2014

33

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

Year:

2018

Language:

english

File:

PDF, 455 KB

english, 2018

34

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

Year:

2017

File:

PDF, 551 KB

2017

35

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

Year:

2015

Language:

english

File:

PDF, 585 KB

english, 2015

36

Glucose phosphate isomerase (GPI) Tadikonda: Characterization of a novel Pro340Ser mutation

Zaidi, Ahmar U., Kedar, Prabhakar, Koduri, Prasad Rao, Goyette, Gerard W., Buck, Steven, Paglia, Donald E., Ravindranath, Yaddanapudi

Journal:

Pediatric Hematology-Oncology

Year:

2017

Language:

english

File:

PDF, 781 KB

english, 2017

37

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

Year:

2020

Language:

english

File:

PDF, 1.09 MB

english, 2020

38

Effect of Pb addition on dielectric relaxation in Se80In20 glassy system

Ram, Indra Sen, Singh, Rajesh Kumar, Singh, Prabhakar, Singh, Kedar

Journal:

Journal of Alloys and Compounds

Year:

2013

Language:

english

File:

PDF, 1.53 MB

english, 2013

39

Electrical conduction mechanism in Se 90-x Te 5 Sn 5 In x (x = 0, 3, 6 and 9) multi-component glassy alloys

Ram, Indra Sen, Kumar, Sunil, Singh, Rajesh Kumar, Singh, Prabhakar, Singh, Kedar

Journal:

Year:

2015

Language:

english

File:

PDF, 2.08 MB

english, 2015

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