Search Results - Mehta, Timir

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  1. 1
    Association of HLA-BFNx011502 allele and carbamazepine-induced Stevens-Johnson syndrome among Indians

    Association of HLA-BFNx011502 allele and carbamazepine-induced Stevens-Johnson syndrome among Indians by Mehta, Timir, Prajapati, Laxman, Mittal, Bharti, Joshi, Chaitanya, Sheth, Jayesh, Patel, Dinesh, Dave, Dinkar, Goyal, Ramesh

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  2. 2
    Association of HLA-B1502 allele and carbamazepine-induced Stevens-Johnson syndrome among Indians

    Association of HLA-B1502 allele and carbamazepine-induced Stevens-Johnson syndrome among Indians by Mehta, Timir Y, Prajapati, Laxman M, Mittal, Bharti, Joshi, Chaitanya G, Sheth, Jayesh J, Patel, Dinesh B, Dave, Dinkar M, Goyal, Ramesh K

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  3. 3
    Expanding the spectrum of γ-secretase gene mutation-associated phenotypes: two novel mutations segregating with familial hidradenitis suppurativa (acne inversa) and acne conglobata

    Expanding the spectrum of γ-secretase gene mutation-associated phenotypes: two novel mutations segregating with familial hidradenitis suppurativa (acne inversa) and acne conglobata... by Ratnamala, Uppala, Jhala, Devendrasinh, Jain, Nayan K., Saiyed, Nazia M., Raveendrababu, Meda, Rao, Mandava V., Mehta, Timir Y., Al-Ali, Faiza M., Raval, Kavi, Nair, Sreelatha, Chandramohan, Nair K., Kuracha, Murali R., Nath, Swapan K., Radhakrishna, Uppala

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  4. 4
    Hidradenitis suppurativa (or Acne inversa) with autosomal dominant inheritance is not linked to chromosome 1p21.1-1q25.3 region

    Hidradenitis suppurativa (or Acne inversa) with autosomal dominant inheritance is not linked to chromosome 1p21.1-1q25.3 region by Saleh Al-Ali, Faiza Mohamed, Ratnamala, Uppala, Mehta, Timir Y., Naveed, Mohammad, Al-Ali, Mahmoud T., Al-Khaja, Najib, Sheth, Jayesh J., Master, Dilipkumar C., Maiti, Amit K., Chetan, Ghati K., Nath, Swapan K., Radhakrishna, Uppala

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  5. 5
    History of IADVL (1973- 2009)

    History of IADVL (1973- 2009) by Mehta, Timir, Marfatia, Y

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  6. 6
    Genetic analysis of three large Indian pedigrees with autosomal dominant hidradenitis suppurativa

    Genetic analysis of three large Indian pedigrees with autosomal dominant hidradenitis suppurativa by Radhakrishna, Uppala, Mehta, Timir Y., Solanki, Jitendra V., Nath, Swapan K.

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  7. 7
    The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region

    The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region by Radhakrishna, Uppala, Blouin, Jean-Louis, Mehenni, Hamid, Mehta, Timir Y., Sheth, Frenny J., Sheth, Jayesh J., Solanki, Jitendra V., Antonarakis, Stylianos E.

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  8. 8
    The future of hypertension pharmacotherapy: Ongoing and future clinical trials for hypertension

    The future of hypertension pharmacotherapy: Ongoing and future clinical trials for hypertension by Mansoor, Taha, Farrukh, Fatima, Khalid, Subaina N., Abramov, Dmitry, Michos, Erin D., Mehta, Anurag, Paul, Timir K., Dani, Sourbha S., Al Rifai, Mahmoud, Misra, Arunima, Nambi, Vijay, Virani, Salim S., Minhas, Abdul Mannan Khan

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  9. 9
    The Fourth Bioelectronic Medicine Summit "Technology Targeting Molecular Mechanisms": current progress, challenges, and charting the future

    The Fourth Bioelectronic Medicine Summit "Technology Targeting Molecular Mechanisms": current progress, challenges, and charting the future by Datta-Chaudhuri, Timir, Zanos, Theodoros, Chang, Eric H, Olofsson, Peder S, Bickel, Stephan, Bouton, Chad, Grande, Daniel, Rieth, Loren, Aranow, Cynthia, Bloom, Ona, Mehta, Ashesh D, Civillico, Gene, Stevens, Molly M, Głowacki, Eric, Bettinger, Christopher, Schüettler, Martin, Puleo, Chris, Rennaker, Robert, Mohanta, Saroj, Carnevale, Daniela, Conde, Silvia V, Bonaz, Bruno, Chernoff, David, Kapa, Suraj, Berggren, Magnus, Ludwig, Kip, Zanos, Stavros, Miller, Larry, Weber, Doug, Yoshor, Daniel, Steinman, Lawrence, Chavan, Sangeeta S, Pavlov, Valentin A, Al-Abed, Yousef, Tracey, Kevin J

    Published in Bioelectronic medicine
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