Search

Your search keyword '"Chakera, Ali J."' showing total 6 results
Start Over Author "Chakera, Ali J." Database OAIster
6 results on '"Chakera, Ali J."'

1. tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in human

Author

Igoillo Esteve, Mariana, Genin, Anne, Lambert, Nelle, Désir, Julie, Pirson, Isabelle, Abdulkarim, Baroj, Simonis, Nicolas, Drielsma, Anaïs, Marselli, Lorella, Marchetti, Piero, Vanderhaeghen, Pierre, Eizirik, Decio L., Wuyts, Wim, Julier, Cécile, Chakera, Ali J, Ellard, Sian, Hattersley, Andrew T, Abramowicz, Marc, Cnop, Miriam, Igoillo Esteve, Mariana, Genin, Anne, Lambert, Nelle, Désir, Julie, Pirson, Isabelle, Abdulkarim, Baroj, Simonis, Nicolas, Drielsma, Anaïs, Marselli, Lorella, Marchetti, Piero, Vanderhaeghen, Pierre, Eizirik, Decio L., Wuyts, Wim, Julier, Cécile, Chakera, Ali J, Ellard, Sian, Hattersley, Andrew T, Abramowicz, Marc, and Cnop, Miriam

Abstract

SCOPUS: ar.j, info:eu-repo/semantics/published

Published
2013

2. tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans

Author

Belgian Medical Genomics Initiative (BeMGI) Kickoff Meeting (2013: Leuven, Belgium), Igoillo Esteve, Mariana, Genin, Anne, Lambert, Nelle, Désir, Julie, Pirson, Isabelle, Abdulkarim, Baroj, Simonis, Nicolas, Drielsma, Anaïs, Marselli, Lorella, Marchetti, Piero, Vanderhaeghen, Pierre, Eizirik, Decio L., Wuyts, Wim, Julier, Cécile, Chakera, Ali J, Ellard, Sian, Hattersley, Andrew T, Abramowicz, Marc, Belgian Medical Genomics Initiative (BeMGI) Kickoff Meeting (2013: Leuven, Belgium), Igoillo Esteve, Mariana, Genin, Anne, Lambert, Nelle, Désir, Julie, Pirson, Isabelle, Abdulkarim, Baroj, Simonis, Nicolas, Drielsma, Anaïs, Marselli, Lorella, Marchetti, Piero, Vanderhaeghen, Pierre, Eizirik, Decio L., Wuyts, Wim, Julier, Cécile, Chakera, Ali J, Ellard, Sian, Hattersley, Andrew T, and Abramowicz, Marc

Abstract

info:eu-repo/semantics/nonPublished

Published
2013

3. Loss-of-function of TRMT10A causes young onset diabetes and microcephaly

Author

23rd Meeting of the Belgian Endocrine Society (2013: Ghent, Belgium), Igoillo Esteve, Mariana, Genin, Anne, Lambert, Nelle, Désir, Julie, Pirson, Isabelle, Abdulkarim, Baroj, Simonis, Nicolas, Drielsma, Anaïs, Marselli, Lorella, Marchetti, Piero, Vanderhaeghen, Pierre, Eizirik, Decio L., Wuyts, Wim, Julier, Cécile, Chakera, Ali J, Ellard, Sian, Hattersley, Andrew T, Abramowicz, Marc, 23rd Meeting of the Belgian Endocrine Society (2013: Ghent, Belgium), Igoillo Esteve, Mariana, Genin, Anne, Lambert, Nelle, Désir, Julie, Pirson, Isabelle, Abdulkarim, Baroj, Simonis, Nicolas, Drielsma, Anaïs, Marselli, Lorella, Marchetti, Piero, Vanderhaeghen, Pierre, Eizirik, Decio L., Wuyts, Wim, Julier, Cécile, Chakera, Ali J, Ellard, Sian, Hattersley, Andrew T, and Abramowicz, Marc

Abstract

info:eu-repo/semantics/nonPublished

Published
2013

4. Loss-of-function of TRMT10A causes young onset diabetes and microcephaly

Author

23rd Meeting of the Belgian Endocrine Society (2013: Ghent, Belgium), Igoillo Esteve, Mariana, Genin, Anne, Lambert, Nelle, Désir, Julie, Pirson, Isabelle, Abdulkarim, Baroj, Simonis, Nicolas, Drielsma, Anaïs, Marselli, Lorella, Marchetti, Piero, Vanderhaeghen, Pierre, Eizirik, Decio L., Wuyts, Wim, Julier, Cécile, Chakera, Ali J, Ellard, Sian, Hattersley, Andrew T, Abramowicz, Marc, 23rd Meeting of the Belgian Endocrine Society (2013: Ghent, Belgium), Igoillo Esteve, Mariana, Genin, Anne, Lambert, Nelle, Désir, Julie, Pirson, Isabelle, Abdulkarim, Baroj, Simonis, Nicolas, Drielsma, Anaïs, Marselli, Lorella, Marchetti, Piero, Vanderhaeghen, Pierre, Eizirik, Decio L., Wuyts, Wim, Julier, Cécile, Chakera, Ali J, Ellard, Sian, Hattersley, Andrew T, and Abramowicz, Marc

Abstract

info:eu-repo/semantics/nonPublished

Published
2013

5. tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans

Author

Belgian Medical Genomics Initiative (BeMGI) Kickoff Meeting (2013: Leuven, Belgium), Igoillo Esteve, Mariana, Genin, Anne, Lambert, Nelle, Désir, Julie, Pirson, Isabelle, Abdulkarim, Baroj, Simonis, Nicolas, Drielsma, Anaïs, Marselli, Lorella, Marchetti, Piero, Vanderhaeghen, Pierre, Eizirik, Decio L., Wuyts, Wim, Julier, Cécile, Chakera, Ali J, Ellard, Sian, Hattersley, Andrew T, Abramowicz, Marc, Belgian Medical Genomics Initiative (BeMGI) Kickoff Meeting (2013: Leuven, Belgium), Igoillo Esteve, Mariana, Genin, Anne, Lambert, Nelle, Désir, Julie, Pirson, Isabelle, Abdulkarim, Baroj, Simonis, Nicolas, Drielsma, Anaïs, Marselli, Lorella, Marchetti, Piero, Vanderhaeghen, Pierre, Eizirik, Decio L., Wuyts, Wim, Julier, Cécile, Chakera, Ali J, Ellard, Sian, Hattersley, Andrew T, and Abramowicz, Marc

Abstract

info:eu-repo/semantics/nonPublished

Published
2013

6. Treatment for primary hypothyroidism: current approaches and future possibilities

Author

Chakera,Ali J, Pearce,Simon HS, Vaidya,Bijay, Chakera,Ali J, Pearce,Simon HS, and Vaidya,Bijay

Abstract

Ali J Chakera1, Simon HS Pearce2, Bijay Vaidya11Department of Endocrinology, Royal Devon and Exeter Hospital and Peninsula Medical School, Exeter, 2Endocrine Unit, Royal Victoria Infirmary and Newcastle University, Newcastle upon Tyne, UKAbstract: Primary hypothyroidism is the most common endocrine disease. Although the diagnosis and treatment of hypothyroidism is often considered simple, there are large numbers of people with this condition who are suboptimally treated. Even in those people with hypothyroidism who are biochemically euthyroid on levothyroxine replacement there is a significant proportion who report poorer quality of life. This review explores the historical and current treatment options for hypothyroidism, reasons for and potential solutions to suboptimal treatment, and future possibilities in the treatment of hypothyroidism.Keywords: primary hypothyroidism, levothyroxine, triiodothyronine, thyroid-stimulating hormone, thyroid

Published
2011

Catalog

Books, media, physical & digital resources
See catalog results