Items where Author is "Makani, Julie"
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Africa
Cox, Sharon E. ORCID: 0000-0002-9908-2936 , Makani, Julie ORCID: 0000-0002-4801-6250 , Soka, Deogratias, L'Esperence, Veline S., Kija, Edward, Dominguez Salas, Paula ORCID: 0000-0001-8753-4221 , Newton, Charles R. J., Birch, Anthony A., Prentice, Andrew M. and Kirkham, Fenella J. (2014) Haptoglobin, alpha‐thalassaemia and glucose‐6‐phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania. British Journal of Haematology, 165 (5). pp. 699-706. ISSN 0007-1048 (Print), 1365-2141 (Online) (doi:https://doi.org/10.1111/bjh.12791)
cerebral blood flow velocity
Cox, Sharon E. ORCID: 0000-0002-9908-2936 , Makani, Julie ORCID: 0000-0002-4801-6250 , Soka, Deogratias, L'Esperence, Veline S., Kija, Edward, Dominguez Salas, Paula ORCID: 0000-0001-8753-4221 , Newton, Charles R. J., Birch, Anthony A., Prentice, Andrew M. and Kirkham, Fenella J. (2014) Haptoglobin, alpha‐thalassaemia and glucose‐6‐phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania. British Journal of Haematology, 165 (5). pp. 699-706. ISSN 0007-1048 (Print), 1365-2141 (Online) (doi:https://doi.org/10.1111/bjh.12791)
children
Cox, Sharon E. ORCID: 0000-0002-9908-2936 , Makani, Julie ORCID: 0000-0002-4801-6250 , Soka, Deogratias, L'Esperence, Veline S., Kija, Edward, Dominguez Salas, Paula ORCID: 0000-0001-8753-4221 , Newton, Charles R. J., Birch, Anthony A., Prentice, Andrew M. and Kirkham, Fenella J. (2014) Haptoglobin, alpha‐thalassaemia and glucose‐6‐phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania. British Journal of Haematology, 165 (5). pp. 699-706. ISSN 0007-1048 (Print), 1365-2141 (Online) (doi:https://doi.org/10.1111/bjh.12791)
non-communicable diseases
Bukhman, Gene, Mocumbi, Ana O, Atun, Rifat, Becker, Anne E, Bhutta, Zulfiqar, Binagwaho, Agnes, Clinton, Chelsea, Coates, Matthew M, Dain, Katie, Ezzati, Majid, Gottlieb, Gary, Gupta, Indrani, Gupta, Neil, Hyder, Adnan A, Jain, Yogesh, Kruk, Margaret E, Makani, Julie, Marx, Andrew, Miranda, J Jaime, Norheim, Ole F, Nugent, Rachel, Roy, Nobhojit, Stefan, Cristina, Wallis, Lee, Mayosi, Bongani, Adjaye-Gbewonyo, Kafui ORCID: 0000-0002-8919-6518 , Adler, Alma, Amegashie, Fred, Amuyunzu-Nyamongo, Mary Kigasia, Arwal, Said Habib, Bassoff, Nicole, Beste, Jason A., Boudreaux, Chantelle, Byass, Peter, Cadet, Jean Roland, Dagnaw, Wubaye Walelgne, Eagan, Arielle Wilder, Feigl, Andrea, Gathecha, Gladwell, Haakenstad, Annie, Haileamlak, Abraham Mitike, Johansson, Kjell Arne, Kamanda, Mamusu, Karmacharya, Biraj, Kasomekera, Noel, Kintu, Alex, Koirala, Bhagawan, Kwan, Gene F., Larco, Nancy Charles, Maongezi, Sarah, Masiye, Jones, Mayige, Mary, McLaughlin, Amy, Memirie, Solomon Tessema, Muquingue, Humberto Nelson, Mwangi, Kibachio Joseph Muiruri, Ndayisaba, Gilles Francois, Noble, Christopher A., Noormal, Bashir, Olsen, Maia, Park, Paul, Aguilar, Gisela Robles, Sankoh, Osman A., Saxena, Akshar, Schwartz, Leah N., Schwarz, Dan K., Shaffer, Jonathan D., Sumner, Andrew P., Doe, Zoe Taylor, Upreti, Senendra Raj, Verguet, Stéphane, Watkins, David and Wroe, Emily B. (2020) The Lancet NCDI Poverty Commission: bridging a gap in universal health coverage for the poorest billion. The Lancet, 396 (10256). pp. 991-1044. ISSN 0140-6736 (Print), 1474-547X (Online) (doi:https://doi.org/10.1016/S0140-6736(20)31907-3)
poverty
Bukhman, Gene, Mocumbi, Ana O, Atun, Rifat, Becker, Anne E, Bhutta, Zulfiqar, Binagwaho, Agnes, Clinton, Chelsea, Coates, Matthew M, Dain, Katie, Ezzati, Majid, Gottlieb, Gary, Gupta, Indrani, Gupta, Neil, Hyder, Adnan A, Jain, Yogesh, Kruk, Margaret E, Makani, Julie, Marx, Andrew, Miranda, J Jaime, Norheim, Ole F, Nugent, Rachel, Roy, Nobhojit, Stefan, Cristina, Wallis, Lee, Mayosi, Bongani, Adjaye-Gbewonyo, Kafui ORCID: 0000-0002-8919-6518 , Adler, Alma, Amegashie, Fred, Amuyunzu-Nyamongo, Mary Kigasia, Arwal, Said Habib, Bassoff, Nicole, Beste, Jason A., Boudreaux, Chantelle, Byass, Peter, Cadet, Jean Roland, Dagnaw, Wubaye Walelgne, Eagan, Arielle Wilder, Feigl, Andrea, Gathecha, Gladwell, Haakenstad, Annie, Haileamlak, Abraham Mitike, Johansson, Kjell Arne, Kamanda, Mamusu, Karmacharya, Biraj, Kasomekera, Noel, Kintu, Alex, Koirala, Bhagawan, Kwan, Gene F., Larco, Nancy Charles, Maongezi, Sarah, Masiye, Jones, Mayige, Mary, McLaughlin, Amy, Memirie, Solomon Tessema, Muquingue, Humberto Nelson, Mwangi, Kibachio Joseph Muiruri, Ndayisaba, Gilles Francois, Noble, Christopher A., Noormal, Bashir, Olsen, Maia, Park, Paul, Aguilar, Gisela Robles, Sankoh, Osman A., Saxena, Akshar, Schwartz, Leah N., Schwarz, Dan K., Shaffer, Jonathan D., Sumner, Andrew P., Doe, Zoe Taylor, Upreti, Senendra Raj, Verguet, Stéphane, Watkins, David and Wroe, Emily B. (2020) The Lancet NCDI Poverty Commission: bridging a gap in universal health coverage for the poorest billion. The Lancet, 396 (10256). pp. 991-1044. ISSN 0140-6736 (Print), 1474-547X (Online) (doi:https://doi.org/10.1016/S0140-6736(20)31907-3)
sickle cell anaemia
Cox, Sharon E. ORCID: 0000-0002-9908-2936 , Makani, Julie ORCID: 0000-0002-4801-6250 , Soka, Deogratias, L'Esperence, Veline S., Kija, Edward, Dominguez Salas, Paula ORCID: 0000-0001-8753-4221 , Newton, Charles R. J., Birch, Anthony A., Prentice, Andrew M. and Kirkham, Fenella J. (2014) Haptoglobin, alpha‐thalassaemia and glucose‐6‐phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania. British Journal of Haematology, 165 (5). pp. 699-706. ISSN 0007-1048 (Print), 1365-2141 (Online) (doi:https://doi.org/10.1111/bjh.12791)
sickle cell disease
Cox, Sharon E. ORCID: 0000-0002-9908-2936 , Makani, Julie ORCID: 0000-0002-4801-6250 , Soka, Deogratias, L'Esperence, Veline S., Kija, Edward, Dominguez Salas, Paula ORCID: 0000-0001-8753-4221 , Newton, Charles R. J., Birch, Anthony A., Prentice, Andrew M. and Kirkham, Fenella J. (2014) Haptoglobin, alpha‐thalassaemia and glucose‐6‐phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania. British Journal of Haematology, 165 (5). pp. 699-706. ISSN 0007-1048 (Print), 1365-2141 (Online) (doi:https://doi.org/10.1111/bjh.12791)
Tanzania
Cox, Sharon E. ORCID: 0000-0002-9908-2936 , Makani, Julie ORCID: 0000-0002-4801-6250 , Soka, Deogratias, L'Esperence, Veline S., Kija, Edward, Dominguez Salas, Paula ORCID: 0000-0001-8753-4221 , Newton, Charles R. J., Birch, Anthony A., Prentice, Andrew M. and Kirkham, Fenella J. (2014) Haptoglobin, alpha‐thalassaemia and glucose‐6‐phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania. British Journal of Haematology, 165 (5). pp. 699-706. ISSN 0007-1048 (Print), 1365-2141 (Online) (doi:https://doi.org/10.1111/bjh.12791)