Parag M Tamhankar: search on Z-Library

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1

A Novel Approach for Character Segmentation of Offline Handwritten Marathi Documents written in MODI Script

Tamhankar, Parag A., Masalkar, Krishnat D., kolhe, Satish R.

Journal:

Procedia Computer Science

Year:

2020

File:

PDF, 1.34 MB

2020

2

Prevention of homozygous beta thalassemia by premarital screening and prenatal diagnosis in India

Parag M. Tamhankar, Sarita Agarwal, Vandana Arya, Ravindra Kumar, U. R. Gupta, S. S. Agarwal

Journal:

Prenatal Diagnosis

Year:

2009

Language:

english

File:

PDF, 145 KB

english, 2009

3

Can indian classical instrumental music reduce pain felt during venepuncture?

Parag M. Tamhankar, Vasundhara S. Chennuri, Rajiv Balan, Nithya Gogtay, S.B. Bavdekar

Journal:

Indian Journal of Pediatrics

Year:

2010

Language:

english

File:

PDF, 57 KB

english, 2010

4

Molecular and clinical heterogeneity in CLCN7-dependent osteopetrosis: report of 20 novel mutations

Alessandra Pangrazio, Michael Pusch, Elena Caldana, Annalisa Frattini, Edoardo Lanino, Parag M Tamhankar, Shubha Phadke, Antonio Gonzalez Meneses Lopez, Paul Orchard, Ercan Mihci, Mario Abinun, Michae

Journal:

Year:

2010

Language:

english

File:

PDF, 184 KB

english, 2010

5

A novel beta-globin mutation (HBB:c.107A>G; or codon 35

Ravindra Kumar, Parag M. Tamhankar, Inusha Panigrahi, Ashwin Dalal, Sarita Agarwal

Journal:

Annals of Hematology

Year:

2009

Language:

english

File:

PDF, 88 KB

english, 2009

6

Hemorrhagic pleural effusion: Can it be scurvy?

Jyoti Suvarna, Parag M. Tamhankar, C. T. Deshmukh

Journal:

Indian Journal of Pediatrics

Year:

2007

Language:

english

File:

PDF, 104 KB

english, 2007

7

Identification ofDKC1gene mutation in an Indian patient

Parag M. Tamhankar, Meina Zhao, Hirokazu Kanegane, Shubha R. Phadke

Journal:

Indian Journal of Pediatrics

Year:

2010

Language:

english

File:

PDF, 119 KB

english, 2010

8

Lack of association of primary iron overload and common HFE gene mutations with liver cirrhosis in adult Indian population

Shalu Jain, Sarita Agarwal, Parag Tamhankar, Prashant Verma, Gourdas Choudhuri

Journal:

Indian Journal of Gastroenterology

Year:

2011

Language:

english

File:

PDF, 115 KB

english, 2011

9

Profile of patients with Von Gierke disease from India

Tamhankar, Parag M., Boggula, Vijayraju, Girisha, K. M., Phadke, Shubha R.

Journal:

Indian Pediatrics

Year:

2012

Language:

english

File:

PDF, 500 KB

english, 2012

10

Diagnosis of Down Syndrome and Detection of Origin of Nondisjunction by Short Tandem Repeat Analysis

Jain, Shalu, Agarwal, Sarita, Panigrahi, Inusha, Tamhankar, Parag, Phadke, Shubha

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2010

Language:

english

File:

PDF, 3.04 MB

english, 2010

11

Molecular diagnosis of genodermatoses in india

Tamhankar, Parag

Journal:

Molecular Cytogenetics

Year:

2014

Language:

english

File:

PDF, 70 KB

english, 2014

12

Molecular basis of lysosomal storage disorders in India

Kondurkar, Shweta P, Tamhankar, Parag, Kondurkar, Pratima, Dalal, Ashwin, Sheth, Jayesh

Journal:

Molecular Cytogenetics

Year:

2014

Language:

english

File:

PDF, 69 KB

english, 2014

13

Neonatal Severe Hyperparathyroidism due to Compound Heterozygous Mutation of Calcium Sensing Receptor (CaSR) Gene Presenting as Encephalopathy

Kulkarni, Abhishek, Mohite, Mahesh, Vijaykumar, Ramaa, Bansode, Prasanna, Murade, Sachin, Tamhankar, Parag M.

Journal:

Indian Journal of Pediatrics

Year:

2014

Language:

english

File:

PDF, 88 KB

english, 2014

14

Case Reports

Ramzan, Mohammed, Yadav, Satya Prakash, Joshi, Rajesh, Das, Dhanjit, Tamhankar, Parag, Shaikh, Shakil, Agrawal, Amit, Shrivastava, Jyotsna, Singh, Akhil, Choudhary, Shyama, Berwal, Pramod K., Khichar,

Journal:

Indian Pediatrics

Year:

2014

Language:

english

File:

PDF, 591 KB

english, 2014

15

Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease

Ankleshwaria, Chitra, Mistri, Mehul, Bavdekar, Ashish, Muranjan, Mamta, Dave, Usha, Tamhankar, Parag, Khanna, Varun, Jasinge, Eresha, Nampoothiri, Sheela, Edayankara Kadangot, Suresh, Sheth, Frenny, G

Journal:

Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 643 KB

english, 2014

16

Clinical Applications and Implications of Common and Founder Mutations in Indian Subpopulations

Ankala, Arunkanth, Tamhankar, Parag M., Valencia, C. Alexander, Rayam, Krishna K., Kumar, Manisha M., Hegde, Madhuri R.

Journal:

Year:

2015

Language:

english

File:

PDF, 195 KB

english, 2015

17

Prenatal diagnosis in India is not limited to sex selection

Dalal, Ashwin B., Ranganath, Prajnya, Phadke, Shubha R., Kabra, Madhulika, Danda, Sumita, Puri, Ratna Dua, V.H., Sankar, Gupta, Neerja, Patil, S.J., Mandal, Kausik, Tamhankar, Parag, Aggarwal, Shagun,

Journal:

Genetics in Medicine

Year:

2015

Language:

english

File:

PDF, 311 KB

english, 2015

18

Identification of Novel ROR2 Gene Mutations in Indian Children with Robinow Syndrome

Tamhankar, Parag M, Vasudevan, Lakshmi, Kondurkar, Shweta, K, Yashaswini, Agarwalla, Sunil Kumar, Nair, Mohandas, TV, Ramkumar, Chauba, Nitin, Chennuri, Vasundhara Sridhar

Journal:

Journal of Clinical Research in Pediatric Endocrinology

Year:

2014

Language:

english

File:

PDF, 102 KB

english, 2014

19

Chronic myeloid leukemia in case of Klinefelter syndrome

Kashyap, Rajesh, Tamhankar, Parag, Phadke, Subha, Chennuri, Vasundhara

Journal:

Indian Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 324 KB

english, 2014

20

Lipoid proteinosis: Histopathological characterization of early papulovesicular lesions

Khopkar, Uday, Sanghvi, Swapnil, Tamhankar, Parag, Gutte, Rameshwar

Journal:

Indian Dermatology Online Journal

Year:

2012

Language:

english

File:

PDF, 1.80 MB

english, 2012

21

Lenz-Majewski syndrome: Report of a case with novel mutation in PTDSS1 gene

Tamhankar, Parag M., Vasudevan, Lakshmi, Bansal, Vandana, Menon, Shyla R., Gawde, Harshavardhan M., D'Souza, Aruna, Babu, Shiny, Kondurkar, Shweta, Adhia, Rashmi, Das, Dhanjit Kumar

Journal:

European Journal of Medical Genetics

Year:

2015

File:

PDF, 4 KB

2015

22

Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease

Ankleshwaria, Chitra, Mistri, Mehul, Bavdekar, Ashish, Muranjan, Mamta, Dave, Usha, Tamhankar, Parag, Khanna, Varun, Jasinge, Eresha, Nampoothiri, Sheela, Edayankara Kadangot, Suresh, Sheth, Frenny, G

Journal:

Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 63 KB

english, 2015

23

Rubinstein Taybi Syndrome in an Indian Child due toEP300Gene Mutation

Tamhankar, Parag M., Merchant, Rashid, Shah, Ami

Journal:

Indian Journal of Pediatrics

Year:

2016

Language:

english

File:

PDF, 528 KB

english, 2016

24

Clinical, biochemical and mutation profile in Indian patients with Sandhoff disease

Tamhankar, Parag M, Mistri, Mehul, Kondurkar, Pratima, Sanghavi, Daksha, Sheth, Jayesh

Journal:

Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 216 KB

english, 2015

25

Cutaneous mastocytosis. Getting beneath the skin of the issue: a case report

Tamhankar, Parag M, Suvarna, Jyoti, Deshmukh, Chandrahas T

Journal:

Year:

2009

Language:

english

File:

PDF, 2.59 MB

english, 2009

26

Identification of Novel Mutations in HEXA Gene in Children Affected with Tay Sachs Disease from India

Mistri, Mehul, Tamhankar, Parag M., Sheth, Frenny, Sanghavi, Daksha, Kondurkar, Pratima, Patil, Swapnil, Idicula-Thomas, Susan, Gupta, Sarita, Sheth, Jayesh, Schuelke, Markus

Journal:

Year:

2012

Language:

english

File:

PDF, 5.00 MB

english, 2012

27

A Novel Hypomorphic CSF1R Gene Mutation in the Biallelic State Leading to Fatal Childhood Neurodegeneration

Tamhankar, Parag Mohan, Zhu, Bin, Tamhankar, Vasundhara Parag, Mithbawkar, Shilpa, Seabra, Luis, Livingston, John H., Ikeuchi, Takeshi, Crow, Yanick J.

Journal:

Neuropediatrics

Year:

2020

File:

PDF, 1.21 MB

2020

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