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Items: 1 to 20 of 23

1.

Acquired Von Willebrand Syndrome Secondary to Langerhans Cell Histiocytosis.

Radhakrishnan N, Dass J.

Indian J Pediatr. 2020 Jan 3. doi: 10.1007/s12098-019-03139-4. [Epub ahead of print] No abstract available.

PMID:
31900848
2.

IgA-mediated autoimmune hemolytic anemia in an infant.

Radhakrishnan N, Dua S, Arora S.

Transfus Apher Sci. 2019 Dec 13:102695. doi: 10.1016/j.transci.2019.102695. [Epub ahead of print]

PMID:
31862428
3.

Genomics of rare genetic diseases-experiences from India.

GUaRDIAN Consortium, Sivasubbu S, Scaria V.

Hum Genomics. 2019 Sep 25;14(1):52. doi: 10.1186/s40246-019-0215-5. Review.

4.

Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2.

Klemann C, Camacho-Ordonez N, Yang L, Eskandarian Z, Rojas-Restrepo JL, Frede N, Bulashevska A, Heeg M, Al-Ddafari MS, Premm J, Seidl M, Ammann S, Sherkat R, Radhakrishnan N, Warnatz K, Unger S, Kobbe R, Hüfner A, Leahy TR, Ip W, Burns SO, Fliegauf M, Grimbacher B.

Front Immunol. 2019 Mar 19;10:297. doi: 10.3389/fimmu.2019.00297. eCollection 2019.

5.

X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world.

El-Sayed ZA, Abramova I, Aldave JC, Al-Herz W, Bezrodnik L, Boukari R, Bousfiha AA, Cancrini C, Condino-Neto A, Dbaibo G, Derfalvi B, Dogu F, Edgar JDM, Eley B, El-Owaidy RH, Espinosa-Padilla SE, Galal N, Haerynck F, Hanna-Wakim R, Hossny E, Ikinciogullari A, Kamal E, Kanegane H, Kechout N, Lau YL, Morio T, Moschese V, Neves JF, Ouederni M, Paganelli R, Paris K, Pignata C, Plebani A, Qamar FN, Qureshi S, Radhakrishnan N, Rezaei N, Rosario N, Routes J, Sanchez B, Sediva A, Seppanen MR, Serrano EG, Shcherbina A, Singh S, Siniah S, Spadaro G, Tang M, Vinet AM, Volokha A, Sullivan KE.

World Allergy Organ J. 2019 Mar 22;12(3):100018. doi: 10.1016/j.waojou.2019.100018. eCollection 2019.

6.

Consensus Statement of the Indian Academy of Pediatrics in Diagnosis and Management of Hemophilia.

Sachdeva A, Gunasekaran V, Ramya HN, Dass J, Kotwal J, Seth T, Das S, Garg K, Kalra M, Sirisha RS, Prakash A; ‘Consensus in Diagnosis and Management of Hemophilia’ Committee*, Indian Academy of Pediatrics.

Indian Pediatr. 2018 Jul 15;55(7):582-590.

PMID:
30129541
7.

Umbilical Cord Blood Banking: Consensus Statement of the Indian Academy of Pediatrics.

Sachdeva A, Gunasekaran V, Malhotra P, Bhurani D, Yadav SP, Radhakrishnan N, Kalra M, Bhat S, Misra R, Jog P; ‘Guidelines on Umbilical Cord Blood Banking’ Committee of Indian Academy of Pediatrics.

Indian Pediatr. 2018 Jun 15;55(6):489-494.

8.

Cotrimoxazole-induced Methemoglobinemia.

Radhakrishnan N, Rai R.

Indian Pediatr. 2017 Sep 15;54(9):786-787. No abstract available.

PMID:
28984267
9.

Disseminated Cryptococcosis in an Immunocompetent Toddler.

Gupta N, Sachdev A, Gupta D, Radhakrishnan N.

Indian Pediatr. 2017 Feb 15;54(2):145-146.

10.

Characterization of two novel FANCG mutations in Indian Fanconi anemia patients.

Solanki A, Kumar Selvaa C, Sheth F, Radhakrishnan N, Kalra M, Vundinti BR.

Leuk Res. 2017 Feb;53:50-56. doi: 10.1016/j.leukres.2016.11.013. Epub 2016 Nov 29.

PMID:
28024295
11.

Serum Procalcitonin for Predicting Significant Infections and Mortality in Pediatric Oncology.

Gunasekaran V, Radhakrishnan N, Dinand V, Sachdeva A.

Indian Pediatr. 2016 Dec 15;53(12):1075-1078. Epub 2016 Nov 5.

12.

Plasma Epstein Barr virus (EBV) DNA as a biomarker for EBV associated Hodgkin lymphoma.

Dinand V, Sachdeva A, Datta S, Bhalla S, Kalra M, Wattal C, Radhakrishnan N.

Indian Pediatr. 2015 Aug;52(8):681-5.

13.

Kawasaki disease with autoimmune hemolytic anemia.

Thakkar D, Radhakrishnan N, Pruthi PK, Sachdeva A.

Indian Pediatr. 2015 Mar 8;52(3):245-6.

14.

Trisomy chromosome 6 as a sole cytogenetic abnormality in acute myeloid leukemia.

Gupta M, Radhakrishnan N, Mahapatra M, Saxena R.

Turk J Haematol. 2015 Mar 5;32(1):77-9. doi: 10.4274/tjh.2013.0107.

15.

Compound heterozygous hemoglobin d-punjab/hemoglobin d-iran: a novel hemoglobinopathy.

Gupta A, Saraf A, Dass J, Mehta M, Radhakrishnan N, Saxena R, Bhargava M.

Indian J Hematol Blood Transfus. 2014 Sep;30(Suppl 1):409-12. doi: 10.1007/s12288-014-0441-x. Epub 2014 Aug 8.

16.

X-linked hyper IgM syndrome: clinical, immunological and molecular features in patients from India.

Madkaikar M, Gupta M, Chavan S, Italia K, Desai M, Merchant R, Radhakrishnan N, Ghosh K.

Blood Cells Mol Dis. 2014 Sep;53(3):99-104. doi: 10.1016/j.bcmd.2014.05.008. Epub 2014 Jun 11.

PMID:
24929972
17.

Disseminated myeloid sarcomas-a rare presentation of acute myeloid leukemia.

Gupta AK, Radhakrishnan N, Sachdeva A.

Pediatr Hematol Oncol. 2014 Mar;31(2):140-2. doi: 10.3109/08880018.2013.867557.

PMID:
24552499
18.

Diamond blackfan anemia: a tertiary care center experience.

Singh AK, Radhakrishnan N, Seth T, Mishra P, Mahapatra M, Pati H.

Mediterr J Hematol Infect Dis. 2013 Jun 3;5(1):e2013039. doi: 10.4084/MJHID.2013.039. Print 2013.

19.

Intestinal mucormycosis: a rare entity in pediatric oncology.

Radhakrishnan N, Yadav SP, Oberoi J, Kulshreshta R, Bhalla S, Sachdeva A.

Pediatr Hematol Oncol. 2013 Apr;30(3):178-83. doi: 10.3109/08880018.2013.769286. Epub 2013 Feb 14.

PMID:
23410194
20.

Antioxidant levels at diagnosis in childhood acute lymphoblastic leukemia.

Radhakrishnan N, Dinand V, Rao S, Gupta P, Toteja GS, Kalra M, Yadav SP, Sachdeva A.

Indian J Pediatr. 2013 Apr;80(4):292-6. doi: 10.1007/s12098-012-0892-8. Epub 2012 Nov 28.

PMID:
23188708

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