Number needed to treat von Amitabh Biswas

Volltext

Study of microscopic origin of segregation for FexCu1−x and CuxCo1−x liquid binary alloys von Faruk Mir Mehedi, Bhuiyan, G M, Biswas Amitabh, Hossain Md Sazzad

Volltext

Uncovering Potential Susceptibility Genes for Knee Osteoarthritis through Whole Exome Sequencing von Biswas, Amitabh, Garg, Bhavuk

Volltext

704 - Uncovering Potential Susceptibility Genes for Knee Osteoarthritis through Whole Exome Sequencing von Biswas, Amitabh, Garg, Bhavuk

Volltext

Familial Hypertrophic Cardiomyopathy - Identification of cause and risk stratification through exome sequencing von Biswas, Amitabh, Das, Soumi, Kapoor, Mitali, Shamsudheen, Karuthedath Vellarikkal, Jayarajan, Rijith, Verma, Ankit, Seth, Sandeep, Bhargava, Balram, Scaria, Vinod, Sivasubbu, Sridhar, Rao, V.R.

Volltext

Multiple tier detection of TNT using curcumin functionalized silver nanoparticles von Raza, Ali, Biswas, Amitabh, Zehra, Ali, Mengesha, Abdurrohman

Volltext

Outreach program von Shivani Vashista, Amitabh Biswas

Volltext

Story of gene: Part II - Genetics and genomics von Sharma, Pragya, Das, Soumi, Biswas, Amitabh

Volltext

Gait analysis technologies for biomechanical assessment in knee osteoarthritis: Understanding variability and distinctions von Biswas, Amitabh, Gupta, Manish, Garg, Bhavuk

Volltext

Decoding the Genetic Threads of Disc Degeneration von Biswas, Amitabh, Garg, Bhavuk

Volltext

Mutations in Hotspot Region of MYH7 Gene Exon 23 Associated with Restrictive Cardiomyopathy von Kapoor, Mitali, Das, Soumi, Biswas, Amitabh, Seth, Sandeep, Bhargava, Balram, Rao, Vadlamudi Raghavendra

Volltext

Epidemiology of cardiomyopathy - A Clinical and Genetic Study of Restrictive Cardiomyopathy: The EPOCH-R Study von Kapoor, Mitali, Das, Soumi, Biswas, Amitabh, Seth, Sandeep, Bhargava, Balram, Rao, Vadlamudi

Volltext

Epidemiology of cardiomyopathy - A clinical and genetic study of hypertrophic cardiomyopathy: The EPOCH-H study von Amitabh Biswas, Soumi Das, Mitali Kapoor, Sandeep Seth, Balram Bhargava, Vadlamudi Raghavendra Rao

Volltext

Epidemiology of cardiomyopathy - A clinical and genetic study of dilated cardiomyopathy: The EPOCH-D study von Soumi Das, Amitabh Biswas, Mitali Kapoor, Sandeep Seth, Balram Bhargava, Vadlamudi R Rao

Volltext

Story of the gene von Das, Soumi, Biswas, Amitabh

Volltext

Ectodermal dysplasia-skin fragility syndrome - identification of a novel plakophilin1 (PKP1) gene variant through whole exome sequencing von Chandra Konda, Sharath, Biswas, Amitabh, Konda, Amritha, Raghavendra Rao, Vadlamudi, Adepu, Vilas

Volltext

Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy von Biswas, Amitabh, Raza, Ali, Das, Soumi, Kapoor, Mitali, Jayarajan, Rijith, Verma, Ankit, Shamsudheen, Karuthedath Vellarikkal, Murry, Benrithung, Seth, Sandeep, Bhargava, Balram, Scaria, Vinod, Sivasubbu, Sridhar, Rao, Vadlamudi Raghavendra

Volltext

Study of microscopic origin of segregation for Fe x Cu1− x and Cu x Co1− x liquid binary alloys von Faruk, Mir Mehedi, Bhuiyan, G. M., Biswas, Amitabh, Hossain, Md. Sazzad

Volltext

Genomics of rare genetic diseases-experiences from India von Sivasubbu, Sridhar, Scaria, Vinod

Volltext

Study of microscopic origin of segregation for Fe(x)Cu(1-x) and Cu(x)Co(1-x) liquid binary alloys von Faruk, Mir Mehedi, Bhuiyan, G M, Biswas, Amitabh, Hossain, Md Sazzad

Volltext