Search Results - "Amare, Pratibha"

Observation on frequency & clinico-pathological significance of various cytogenetic risk groups in multiple myeloma: an experience from India by Kadam Amare, Pratibha S, Jain, Hemani, Nikalje, Shraddha, Sengar, Manju, Menon, Hari, Inamdar, Nitin, Subramanian, P G, Gujral, Sumeet, Shet, Tanuja, Epari, Sridhar, Nair, Reena

“…Multiple myeloma (MM) is a plasma cell malignancy characterized by cytogenetic heterogeneity. In comparison with conventional karyotyping, fluorescence in situ…”
Get full text

Plasmablastic transformation of a double hit follicular lymphoma: An emerging entity by Khodaiji, Shanaz, Mahajan, Vidisha, Satyakam, Krishna Sawaimoon, Amare, Pratibha Sudhan Kadam

“…Plasmablastic transformation of follicular lymphoma is very rare and has been reported in only 5 cases till date. We report a case of simultaneous…”
Get full text

Investigation of tumor suppressor genes apart from VHL on 3p by deletion mapping in sporadic clear cell renal cell carcinoma (cRCC) by Singh, Rashmi Bhat, Ph.D, Amare Kadam, Pratibha S., Ph.D

“…Abstract Objectives To investigate the most recurrent deletion loci on 3p12-p26 by deletion mapping studies by PCR-LOH and BAC array-FISH in sporadic…”
Get full text

Molecular Heterogeneity in Acute Promyelocytic Leukemia - a Single Center Experience from India by Rabade, Nikhil, Raval, Goutham, Chaudhary, Shruti, Subramanian, P G, Kodgule, Rohan, Joshi, Swapnali, Tembhare, Prashant, Hasan, Syed K, Jain, Hasmukh, Sengar, Manju, Narula, Gaurav, Banavali, Shripad, Kadam, Pratibha Amare, Shetty, Dhanalaxmi, Gujral, Sumeet, Patkar, Nikhil

“…Atypical breakpoints and variant APL cases involving alternative chromosomal aberrations are seen in a small subset of acute promyelocytic leukemia (APL)…”
Get full text

Applicability of 2008 World Health Organization classification system of hematolymphoid neoplasms: Learning experiences by Modkharkar, Sushil, Navale, Pooja, Amare, Pratibha, Chougule, Anuradha, Patkar, Nikhil, Tembhare, Prashant, Menon, Hari, Sengar, Manju, Khattry, Navin, Banavali, Shripad, Arora, Brijesh, Narula, Gaurav, Laskar, Siddhartha, Khanna, Nehal, Muckaden, Mary, Rangarajan, Venkatesh, Agrawal, Archi, Shet, Tanuja, Epari, Sridhar, Subramanian, P, Gujral, Sumeet

“…Background: 2008 World Health Organization (WHO) classification of hematolymphoid neoplasms (HLN) has classified them based on morphology, results of various…”
Get full text

Childhood systemic mastocytosis associated with t (8; 21) (q22; q22) acute myeloid leukemia by Rabade, Nikhil, Tembhare, Prashant, Patkar, Nikhil, Amare, Pratibha, Arora, Brijesh, Subramanian, P, Gujral, Sumeet

“…Systemic mastocytosis (SM) with associated clonal nonmast cell lineage disease is seen in up to 20% cases of SM. SM is uncommon in the pediatric population. T…”
Get full text

Lymphoblastic leukemia with surface light chain restriction: A diagnostic dilemma by Rabade, Nikhil, Bibi, Asma, Ghodke, Kiran, Patkar, Nikhil, Tembhare, Prashant, Amare, Pratibha, Subramanian, P, Gujral, Sumeet

“…Surface light chain expression is a feature of mature B-cell neoplasms. Light chain restriction in precursor B acute lymphoblastic leukemia is infrequently…”
Get full text

Investigation of recurrent deletion loci specific to conventional renal cell carcinoma by comparative allelotyping in major epithelial carcinomas by Bhat Singh, Rashmi R, Amare Kadam, Pratibha S

“…Loss of heterozygosity (LOH) studies were undertaken to investigate the consistently deleted loci/? tumor suppressor gene loci (TSG) on 3p in conventional…”
Get full text

Immunogenetics of chronic lymphocytic leukemia by Patkar, Nikhil, Rabade, Nikhil, Kadam, Pratibha, Mishra, Falguni, Muranjan, Aditi, Tembhare, Prashant, Chaudhary, Shruti, Joshi, Swapnali, Jain, Hasmukh, Dangi, Uma, Bagal, Bhausaheb, Khattry, Navin, Menon, Hari, Gujral, Sumeet, Sengar, Manju, Subramanian, P

“…Introduction: Cytogenetic aberrations as well as presence of IGVH mutations are the underlying reason for clinical heterogeneity in Chronic Lymphocytic…”
Get full text

Transient abnormal myelopoiesis: A case series and review of the literature by Baloda, Vandana, Subramanian, Papagudi G., Badrinath, Yajamanam, Kumar, Ashok, Amare, Pratibha S. Kadam, Banavali, Shripad D., Arora, Brijesh, Gujral, Sumeet

“…Transient abnormal myelopoiesis (TAM) is a rare and unique disorder affecting Down syndrome (DS) newborns. This case series presents 5 cases of Down syndrome…”
Get full text

Over expression of brain and acute leukemia, cytoplasmic and ETS‐related gene is associated with poor outcome in acute myeloid leukemia by Hasan, Syed Khizer, Patkar, Nikhil V., Rajamanickam, Deepan, Gokarn, Anant, Lucena‐Araujo, Antonio R., Tembhare, Prashant, Bagal, Bhausaheb, Kadam Amare, Pratibha, Jain, Hasmukh, Gujral, Sumeet, Sengar, Manju, Subramanian, Papagudi Ganesan, Khattry, Navin

“…The high expression of brain and acute leukemia, cytoplasmic (BAALC) and ETS‐related gene (ERG) has been reported to influence the outcome in acute myeloid…”
Get full text

Burkitt's Leukemia After Treatment of Primary Mediastinal Nonseminomatous Germ Cell Tumor by RAINA, Vinod, MEDHI, Kunjahari, KUMAR, Rajive, PRATIBHA AMARE KADAM, KATARIA, Satyapal, CHOPRA, Anita, KALITA, Dipti

Get full text

Blastic plasmacytoid dendritic cell neoplasm: report of two pediatric cases by Dharmani, Preeti Ashok, Mittal, Neha Manish, Subramanian, P G, Galani, Komal, Badrinath, Yajamanam, Amare, Pratibha, Gujral, Sumeet

“…Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare subtype of acute leukemia that typically follows a highly aggressive clinical course in adults,…”
Get full text

Comparative analysis of routine histology, immunohistochemistry, reverse transcriptase polymerase chain reaction, and fluorescence in situ hybridization in diagnosis of Ewing family of tumors by Jambhekar, Nirmala A, Bagwan, Izhar N, Ghule, Prachi, Shet, Tanuja M, Chinoy, Roshni F, Agarwal, Sandhya, Joshi, Rupali, Amare Kadam, Pratibha S

“…The Ewing family of tumors are often difficult to distinguish from other malignant small round cell tumors, but more than 90% have EWS-FLI1 chimeric…”
Get full text

An integrated genomic profile that includes copy number alterations is highly predictive of minimal residual disease status in childhood precursor B-lineage acute lymphoblastic leukemia by Patkar, Nikhil, Subramanian, P G, Tembhare, Prashant, Mandalia, Sneha, Chaterjee, Gaurav, Rabade, Nikhil, Kodgule, Rohan, Chopra, Karishma, Bibi, Asma, Joshi, Swapnali, Chaudhary, Shruti, Mascerhenas, Russel, Kadam-Amare, Pratibha, Narula, Gaurav, Arora, Brijesh, Banavali, Shripad, Gujral, Sumeet

“…Copy number alterations (CNA) have been described in childhood precursor B-lineage acute lymphoblastic leukemia (B-ALL) which in conjunction with chromosomal…”
Get full text

Characterization of cryptic rearrangements, deletion, complex variants of PML, RARA in acute promyelocytic leukemia by Amare, Pratibha Kadam, Baisane, Chanda, Nair, Reena, Menon, Hari, Banavali, Shripad, Kabre, Sharayu, Gujral, Sumit, Subramaniam, P

“…Acute promyelocytic leukemia (APL) is characterized by a reciprocal translocation t(15;17)(q22;q21) leading to the disruption of Promyelocytic leukemia (PML)…”
Get full text

RUNX1 ABERRATIONS IN ETV6/RUNX1-POSITIVE AND ETV6/RUNX1-NEGATIVE PATIENTS: Its Hemato-Pathological and Prognostic Significance in a Large Cohort (619 Cases) of ALL by Pais, Anurita Peter, Amare Kadam, Pratibha S., Raje, Gauri Chandrakant, Banavali, Shripad, Parikh, Purvish, Kurkure, Purna, Arora, Brijesh, Gujral, Sumit, Kumar, S. Ashok, Badrinath, Y.

“…A large-cohort study (619) of acute lymphoblastic leukemia (ALL) revealed an ETV6/RUNX1 (previously known as TEL/AML1) incidence of 18% in pediatric B-cell…”
Get full text

Morphological spectrum of leukemic mantle cell lymphoma by Rahman, Khaliqur, Subramanian, P G, Kadam, Pratibha Amare, Gadage, Vijaya, Galani, Komal, Mittal, Neha, Ghogale, Sitaram, Badrinath, Yajamanam, Ansari, Rashida, Kushte, Shilpa, Nair, Reena, Sengar, Manju, Menon, Hari, Gujral, Sumeet

“…Leukemic involvement in mantle cell lymphoma (MCL) is common, and can be secondary to nodal or extranodal disease or can be de-novo. There is paucity of…”
Get full text

Darier's disease following radiotherapy for carcinoma of cervix by Chopra, Supriya, Sharma, Vinay, Nischal, K C, Khopkar, Uday, Baisane, Chanda, Amare, Kadam Pratibha

“…Darier-White disease is due to a defect in the ATP2A2 gene encoding the sarcoplasmic/endoplasmic reticulum Ca2+ ATPase (SERCA2b). We report a case of carcinoma…”
Get full text

Chromosomal rearrangement in Down syndrome with acute myeloid leukemia by BAKSHI, Chetana, AMARE, Pratibha, ABHYANKAR, Dhiraj, BAISANE, Chanda, BANAVALI, Shripad, ADVANI, Suresh

“…The incidence of acute leukemia in children with Down syndrome (DS) is high as compared to general population. Recent findings have demonstrated that DS…”
Get full text