Shamima Rahman (S Rahman)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 49

Top Venues

Journal of inherited metabolic disease

Annals of clinical and translational neurology

Communications biology

European journal of neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Michelangelo Mancuso, Maria T Papadopoulou, Yi Shiau Ng, Anna Ardissone, Marcello Bellusci, Enrico Bertini, Lidia Di Vito, Teresinha Evangelista, Carmen Fons, Omar Hikmat, Rita Horvath, Florentine Radelfahr, Cornelia Kornblum, Costanza Lamperti, Laura Licchetta, Maria Judit Molnar, Kristin N Varhaug, Mar O'Callaghan, Ronit M Pressler, Manuel Schiff, Serenella Servidei, Nora Szabo, Gráinne S Gorman, Judith Helen Cross, Shamima Rahman
Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group. European journal of neurology 31 (7) (2024)
Nandaki Keshavan, Michal Minczuk, Carlos Pardo-Hernández, Shamima Rahman
Gene therapy for mitochondrial disorders. Journal of inherited metabolic disease (2024)
Michelangelo Mancuso, Maria T Papadopoulou, Yi Shiau Ng, Anna Ardissone, Marcello Bellusci, Enrico Bertini, Lidia Di Vito, Teresinha Evangelista, Carmen Fons, Omar Hikmat, Rita Horvath, Florentine Radelfahr, Cornelia Kornblum, Costanza Lamperti, Laura Licchetta, Maria Judit Molnar, Kristin N Varhaug, Mar O'Callaghan, Ronit M Pressler, Manuel Schiff, Serenella Servidei, Nora Szabo, Gráinne S Gorman, Judith Helen Cross, Shamima Rahman
Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group. European journal of neurology (2024)
Nandaki Keshavan, Michal Minczuk, Carlos Pardo-Hernández, Shamima Rahman
Gene therapy for mitochondrial disorders. Journal of inherited metabolic disease 47 (1) (2024)
Erle Kristensen, Linda Mathisen, Siren Berland, Claus Klingenberg, Eylert Brodtkorb, Magnhild Rasmussen, Trine Tangeraas, Yngve T Bliksrud, Shamima Rahman, Laurence Albert Bindoff, Omar Hikmat
Epidemiology and natural history of POLG disease in Norway: a nationwide cohort study. Annals of clinical and translational neurology 11 (7) (2024)
Michelangelo Mancuso, Maria T Papadopoulou, Yi Shiau Ng, Anna Ardissone, Marcello Bellusci, Enrico Bertini, Lidia Di Vito, Teresinha Evangelista, Carmen Fons, Omar Hikmat, Rita Horvath, Florentine Radelfahr, Cornelia Kornblum, Costanza Lamperti, Laura Licchetta, Maria Judit Molnar, Kristin N Varhaug, Mar O'Callaghan, Ronit M Pressler, Manuel Schiff, Serenella Servidei, Nora Szabo, Gráinne S Gorman, Judith Helen Cross, Shamima Rahman
Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group. European journal of neurology 31 (7) (2024)
Nandaki Keshavan, Michal Minczuk, Carlos Pardo-Hernández, Shamima Rahman
Gene therapy for mitochondrial disorders. Journal of inherited metabolic disease 47 (1) (2024)
Erle Kristensen, Linda Mathisen, Siren Berland, Claus Klingenberg, Eylert Brodtkorb, Magnhild Rasmussen, Trine Tangeraas, Yngve T Bliksrud, Shamima Rahman, Laurence Albert Bindoff, Omar Hikmat
Epidemiology and natural history of POLG disease in Norway: a nationwide cohort study. Annals of clinical and translational neurology 11 (7) (2024)
Erle Kristensen, Linda Mathisen, Siren Berland, Claus Klingenberg, Eylert Brodtkorb, Magnhild Rasmussen, Trine Tangeraas, Yngve T Bliksrud, Shamima Rahman, Laurence Albert Bindoff, Omar Hikmat
Epidemiology and natural history of POLG disease in Norway: a nationwide cohort study. Annals of clinical and translational neurology 11 (7) (2024)
Martina Messina, Frederic M Vaz, Shamima Rahman
Mitochondrial membrane synthesis, remodelling and cellular trafficking. Journal of inherited metabolic disease (2024)
Michelangelo Mancuso, Maria T Papadopoulou, Yi Shiau Ng, Anna Ardissone, Marcello Bellusci, Enrico Bertini, Lidia Di Vito, Teresinha Evangelista, Carmen Fons, Omar Hikmat, Rita Horvath, Florentine Radelfahr, Cornelia Kornblum, Costanza Lamperti, Laura Licchetta, Maria Judit Molnar, Kristin N Varhaug, Mar O'Callaghan, Ronit M Pressler, Manuel Schiff, Serenella Servidei, Nora Szabo, Gráinne S Gorman, Judith Helen Cross, Shamima Rahman
Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group. European journal of neurology 31 (7) (2024)
Erle Kristensen, Linda Mathisen, Siren Berland, Claus Klingenberg, Eylert Brodtkorb, Magnhild Rasmussen, Trine Tangeraas, Yngve T Bliksrud, Shamima Rahman, Laurence Albert Bindoff, Omar Hikmat
Epidemiology and natural history of POLG disease in Norway: a nationwide cohort study. Annals of clinical and translational neurology 11 (7) (2024)
Erle Kristensen, Linda Mathisen, Siren Berland, Claus Klingenberg, Eylert Brodtkorb, Magnhild Rasmussen, Trine Tangeraas, Yngve T Bliksrud, Shamima Rahman, Laurence Albert Bindoff, Omar Hikmat
Epidemiology and natural history of POLG disease in Norway: a nationwide cohort study. Annals of clinical and translational neurology (2024)
Nandaki Keshavan, Michal Minczuk, Carlos Pardo-Hernández, Shamima Rahman
Gene therapy for mitochondrial disorders. Journal of inherited metabolic disease 47 (1) (2024)
Gabriel Sturm, Kalpita R Karan, Anna S Monzel, Balaji Santhanam, Tanja Taivassalo, Céline Bris, Sarah A Ware, Marissa Cross, Atif Towheed, Albert T Higgins-Chen, Meagan J McManus, Beckey Trinh, Jue Lin, Elissa S Epel, Shamima Rahman, John Vissing, Bruno Grassi, Morgan E Levine, Steve Horvath, Ronald G Haller, Guy Lenaers, Douglas C Wallace, Marie-Pierre St-Onge, Saeed Tavazoie, Vincent Procaccio, Brett A Kaufman, Erin L Seifert, Michio Hirano, Martin Picard
OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases. Communications biology 6 (1) (2023)
Shamima Rahman, David Bick, Richard H Scott
Whole genome sequencing to screen 100 000 newborns for treatable genetic disorders. Journal of inherited metabolic disease 47 (1) (2023)
Shamima Rahman, David Bick, Richard H Scott
Whole genome sequencing to screen 100 000 newborns for treatable genetic disorders. Journal of inherited metabolic disease 47 (1) (2023)
Gabriel Sturm, Kalpita R Karan, Anna S Monzel, Balaji Santhanam, Tanja Taivassalo, Céline Bris, Sarah A Ware, Marissa Cross, Atif Towheed, Albert T Higgins-Chen, Meagan J McManus, Beckey Trinh, Jue Lin, Elissa S Epel, Shamima Rahman, John Vissing, Bruno Grassi, Morgan E Levine, Steve Horvath, Ronald G Haller, Guy Lenaers, Douglas C Wallace, Marie-Pierre St-Onge, Saeed Tavazoie, Vincent Procaccio, Brett A Kaufman, Erin L Seifert, Michio Hirano, Martin Picard
OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases. Communications biology 6 (1) (2023)
Shamima Rahman, David Bick, Richard H Scott
Whole genome sequencing to screen 100 000 newborns for treatable genetic disorders. Journal of inherited metabolic disease 47 (1) (2023)
Shamima Rahman, Marc C Patterson, Verena Peters, Eva Morava, Johannes Zschocke, Matthias R Baumgartner
Guidelines in the JIMD: Evidence-based practice for inherited metabolic disease. Journal of inherited metabolic disease (2023)
Elizabeth M McCormick, Kierstin Keller, Julie P Taylor, Alison J Coffey, Lishuang Shen, Danuta Krotoski, Brian Harding, null null, César Augusto Pinheiro Ferreira Alves, Anna Ardissone, Renkui Bai, Isabella Peixoto de Barcelos, Enrico Bertini, Krista Bluske, John Christodoulou, Amanda R Clause, William C Copeland, George A Diaz, Nazzareno Diodato, Matthew C Dulik, Greg Enns, Annette Feigenbaum, Carl Fratter, Daniele Ghezzi, Amy Goldstein, Andrea Gropman, Richard Haas, Amel Karaa, Mary Kay Koenig, Berrin Monteleone, Sumit Parikh, Belen Perez Duenas, Revathi Rajkumar, Ann Saada, Russell P Saneto, Kate Sergeant, John Shoffner, Conrad Smith, Christine Stanley, Isabelle Thiffault, David Thorburn, Melissa Walker, Douglas Wallace, Lee-Jun Wong, Xiaowu Gai, Marni J Falk, Zarazuela Zolkipli-Cunningham, Shamima Rahman
Expert panel curation of 113 primary mitochondrial disease genes for the Leigh syndrome spectrum. Annals of neurology (2023)
Gabriel Sturm, Kalpita R Karan, Anna S Monzel, Balaji Santhanam, Tanja Taivassalo, Céline Bris, Sarah A Ware, Marissa Cross, Atif Towheed, Albert T Higgins-Chen, Meagan J McManus, Beckey Trinh, Jue Lin, Elissa S Epel, Shamima Rahman, John Vissing, Bruno Grassi, Morgan E Levine, Steve Horvath, Ronald G Haller, Guy Lenaers, Douglas C Wallace, Marie-Pierre St-Onge, Saeed Tavazoie, Vincent Procaccio, Brett A Kaufman, Erin L Seifert, Michio Hirano, Martin Picard
OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases. Communications biology 6 (1) (2023)
Gabriel Sturm, Kalpita R Karan, Anna S Monzel, Balaji Santhanam, Tanja Taivassalo, Céline Bris, Sarah A Ware, Marissa Cross, Atif Towheed, Albert T Higgins-Chen, Meagan J McManus, Beckey Trinh, Jue Lin, Elissa S Epel, Shamima Rahman, John Vissing, Bruno Grassi, Morgan E Levine, Steve Horvath, Ronald G Haller, Guy Lenaers, Douglas C Wallace, Marie-Pierre St-Onge, Saeed Tavazoie, Vincent Procaccio, Brett A Kaufman, Erin L Seifert, Michio Hirano, Martin Picard
OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases. Communications biology 6 (1) (2023)
Gabriel Sturm, Kalpita R Karan, Anna S Monzel, Balaji Santhanam, Tanja Taivassalo, Céline Bris, Sarah A Ware, Marissa Cross, Atif Towheed, Albert T Higgins-Chen, Meagan J McManus, Beckey Trinh, Jue Lin, Elissa S Epel, Shamima Rahman, John Vissing, Bruno Grassi, Morgan E Levine, Steve Horvath, Ronald G Haller, Guy Lenaers, Douglas C Wallace, Marie-Pierre St-Onge, Saeed Tavazoie, Vincent Procaccio, Brett A Kaufman, Erin L Seifert, Michio Hirano, Martin Picard
OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases. Communications biology 6 (1) (2023)
Shamima Rahman, David Bick, Richard H Scott
Whole genome sequencing to screen 100 000 newborns for treatable genetic disorders. Journal of inherited metabolic disease (2023)
Azizia Wahedi, Chandika Soondram, Alan E Murphy, Nathan G Skene, Shamima Rahman
Transcriptomic analyses reveal neuronal specificity of Leigh syndrome associated genes. Journal of inherited metabolic disease (2022)
Azizia Wahedi, Chandika Soondram, Alan E Murphy, Nathan G Skene, Shamima Rahman
Transcriptomic analyses reveal neuronal specificity of Leigh syndrome associated genes. Journal of inherited metabolic disease 46 (2) (2022)
Azizia Wahedi, Chandika Soondram, Alan E Murphy, Nathan G Skene, Shamima Rahman
Transcriptomic analyses reveal neuronal specificity of Leigh syndrome associated genes. Journal of inherited metabolic disease 46 (2) (2022)
Azizia Wahedi, Chandika Soondram, Alan E Murphy, Nathan G Skene, Shamima Rahman
Transcriptomic analyses reveal neuronal specificity of Leigh syndrome associated genes. Journal of inherited metabolic disease (2022)
Rhys Huw Thomas, Amy Hunter, Lyndsey Butterworth, Catherine Feeney, Tracey D Graves, Sarah Holmes, Pushpa Hossain, Jo Lowndes, Jenny Sharpe, Sheela Upadhyaya, Kristin N Varhaug, Marcela Votruba, Russell Wheeler, Kristina Staley, Shamima Rahman
Research priorities for mitochondrial disorders: Current landscape and patient and professional views. Journal of inherited metabolic disease 45 (4) (2022)
Azizia Wahedi, Chandika Soondram, Alan E Murphy, Nathan G Skene, Shamima Rahman
Transcriptomic analyses reveal neuronal specificity of Leigh syndrome associated genes. Journal of inherited metabolic disease (2022)
William L Macken, Micol Falabella, Caroline McKittrick, Chiara Pizzamiglio, Rebecca Ellmers, Kelly Eggleton, Cathy E Woodward, Yogen Patel, Robyn Labrum, null null, Rahul Phadke, Mary M Reilly, Catherine DeVile, Anna Sarkozy, Emma Footitt, James Davison, Shamima Rahman, Henry Houlden, Enrico Bugiardini, Rosaline Quinlivan, Michael G Hanna, Jana Vandrovcova, Robert D S Pitceathly
Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencing. Nature communications 13 (1) (2022)
Katherine R Schon, Rita Horvath, Wei Wei, Claudia Calabrese, Arianna Tucci, Kristina Ibañez, Thiloka Ratnaike, Robert D S Pitceathly, Enrico Bugiardini, Rosaline Quinlivan, Michael G Hanna, Emma Clement, Emma Ashton, John A Sayer, Paul Brennan, Dragana Josifova, Louise Izatt, Carl Fratter, Victoria Nesbitt, Timothy Barrett, Dominic J McMullen, Audrey Smith, Charulata Deshpande, Sarah F Smithson, Richard Festenstein, Natalie Canham, Mark Caulfield, Henry Houlden, Shamima Rahman, Patrick F Chinnery, null null
Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study. BMJ (Clinical research ed.) 375 (2021)
Carlos R Ferreira, Shamima Rahman, Markus Andreas Keller, Johannes Zschocke, null null
An international classification of inherited metabolic disorders (ICIMD). Journal of inherited metabolic disease 44 (1) (2021)
Alistair T Pagnamenta, Wei Wei, Shamima Rahman, Patrick F Chinnery
Biparental inheritance of mitochondrial DNA revisited. Nature reviews. Genetics 22 (8) (2021)
Patrick Forny, Emma Footitt, James E Davison, Amanda Lam, Cathy E Woodward, Spyros Batzios, Sanjay Bhate, Anupam Chakrapani, Maureen Cleary, Paul Gissen, Stephanie Grunewald, Jane A Hurst, Richard Scott, Simon Heales, Thomas S Jacques, Thomas Cullup, Shamima Rahman
Diagnosing Mitochondrial Disorders Remains Challenging in the Omics Era. Neurology. Genetics 7 (3) (2021)
Omar Hikmat, Pirjo Isohanni, Nandaki Keshavan, Matteo P Ferla, Elisa Fassone, Mary-Alice Abbott, Marcello Bellusci, Niklas Darin, David Dimmock, Daniele Ghezzi, Henry Houlden, Federica Invernizzi, Nazreen B Kamarus Jaman, Manju A Kurian, Eva Morava, Karin Naess, Juan Darío Ortigoza-Escobar, Sumit Parikh, Alessandra Pennisi, Giulia Barcia, Karin B Tylleskär, Damien Brackman, Saskia B Wortmann, Jenny C Taylor, Laurence A Bindoff, Vineta Fellman, Shamima Rahman
Expanding the phenotypic spectrum of BCS1L-related mitochondrial disease. Annals of clinical and translational neurology 8 (11) (2021)
null null, Damian Smedley, Katherine R Smith, Antonio Martin, Ellen A Thomas, Ellen M McDonagh, Valentina Cipriani, Jamie M Ellingford, Gavin Arno, Arianna Tucci, Jana Vandrovcova, Georgia Chan, Hywel J Williams, Thiloka Ratnaike, Wei Wei, Kathleen Stirrups, Kristina Ibanez, Loukas Moutsianas, Matthias Wielscher, Anna Need, Michael R Barnes, Letizia Vestito, James Buchanan, Sarah Wordsworth, Sofie Ashford, Karola Rehmström, Emily Li, Gavin Fuller, Philip Twiss, Olivera Spasic-Boskovic, Sally Halsall, R Andres Floto, Kenneth Poole, Annette Wagner, Sarju G Mehta, Mark Gurnell, Nigel Burrows, Roger James, Christopher Penkett, Eleanor Dewhurst, Stefan Gräf, Rutendo Mapeta, Mary Kasanicki, Andrea Haworth, Helen Savage, Melanie Babcock, Martin G Reese, Mark Bale, Emma Baple, Christopher Boustred, Helen Brittain, Anna de Burca, Marta Bleda, Andrew Devereau, Dina Halai, Eik Haraldsdottir, Zerin Hyder, Dalia Kasperaviciute, Christine Patch, Dimitris Polychronopoulos, Angela Matchan, Razvan Sultana, Mina Ryten, Ana L T Tavares, Carolyn Tregidgo, Clare Turnbull, Matthew Welland, Suzanne Wood, Catherine Snow, Eleanor Williams, Sarah Leigh, Rebecca E Foulger, Louise C Daugherty, Olivia Niblock, Ivone U S Leong, Caroline F Wright, Jim Davies, Charles Crichton, James Welch, Kerrie Woods, Lara Abulhoul, Paul Aurora, Detlef Bockenhauer, Alexander Broomfield, Maureen A Cleary, Tanya Lam, Mehul Dattani, Emma Footitt, Vijeya Ganesan, Stephanie Grunewald, Sandrine Compeyrot-Lacassagne, Francesco Muntoni, Clarissa Pilkington, Rosaline Quinlivan, Nikhil Thapar, Colin Wallis, Lucy R Wedderburn, Austen Worth, Teofila Bueser, Cecilia Compton, Charu Deshpande, Hiva Fassihi, Eshika Haque, Louise Izatt, Dragana Josifova, Shehla Mohammed, Leema Robert, Sarah Rose, Deborah Ruddy, Robert Sarkany, Genevieve Say, Adam C Shaw, Agata Wolejko, Bishoy Habib, Gavin Burns, Sarah Hunter, Russell J Grocock, Sean J Humphray, Peter Nick Robinson, Melissa Haendel, Michael A Simpson, Siddharth Banka, Jill Clayton-Smith, Sofia Douzgou, Georgina Hall, Huw B Thomas, Raymond T O'Keefe, Michel Michaelides, Anthony T Moore, Sam Malka, Nikolas Pontikos, Andrew C Browning, Volker Straub, Gráinne Siobhan Gorman, Rita Horvath, Richard Quinton, Andrew M Schaefer, Patrick Yu-Wai-Man, Doug M Turnbull, Robert McFarland, Robert W Taylor, Emer O'Connor, Janice Yip, Katrina Newland, Huw R Morris, James Polke, Nicholas W Wood, Carolyn Campbell, Carme Camps, Kate Gibson, Nils Koelling, Tracy Lester, Andrea H Németh, Claire Palles, Smita Patel, Noemi B A Roy, Arjune Sen, John Taylor, Pilar Cacheiro, Julius O Jacobsen, Eleanor G Seaby, Val Davison, Lyn Chitty, Angela Douglas, Kikkeri Naresh, Dom McMullan, Sian Ellard, I Karen Temple, Andrew D Mumford, Gill Wilson, Phil Beales, Maria Bitner-Glindzicz, Graeme Black, John R Bradley, Paul Brennan, John Burn, Patrick F Chinnery, Perry Mark Elliott, Frances Flinter, Henry Houlden, Melita Irving, William Newman, Shamima Rahman, John A Sayer, Jenny C Taylor, Andrew R Webster, Andrew O M Wilkie, Willem H Ouwehand, F Lucy Raymond, John Chisholm, Sue Hill, David Bentley, Richard H Scott, Tom Fowler, Augusto Rendon, Mark Caulfield
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. The New England journal of medicine 385 (20) (2021)
Eleanor Hay, Louise C Wilson, Bethan Hoskins, Martin P Samuels, Pinki Munot, Shamima Rahman
Biallelic P4HTM variants associated with HIDEA syndrome and mitochondrial respiratory chain complex I deficiency. European journal of human genetics : EJHG 29 (10) (2021)
Robert D S Pitceathly, Nandaki Keshavan, Joyeeta Rahman, Shamima Rahman
Moving towards clinical trials for mitochondrial diseases. Journal of inherited metabolic disease 44 (1) (2020)
Shamima Rahman
Mitochondrial disease in children. Journal of internal medicine 287 (6) (2020)
Wei Wei, Alistair T Pagnamenta, Nicholas Gleadall, Alba Sanchis-Juan, Jonathan Stephens, John Broxholme, Salih Tuna, Christopher A Odhams, null null, null null, Carl Fratter, Ernest Turro, Mark J Caulfield, Jenny C Taylor, Shamima Rahman, Patrick F Chinnery
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans. Nature communications 11 (1) (2020)
Wei Wei, Alistair T Pagnamenta, Nicholas Gleadall, Alba Sanchis-Juan, Jonathan Stephens, John Broxholme, Salih Tuna, Christopher A Odhams, null null, null null, Carl Fratter, Ernest Turro, Mark J Caulfield, Jenny C Taylor, Shamima Rahman, Patrick F Chinnery
Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans. Nature communications 11 (1) (2020)
A C Goldstein, Shamima Rahman
Seeking impact: Global perspectives on outcome measure selection for translational and clinical research for primary mitochondrial disorders. Journal of inherited metabolic disease 44 (2) (2020)
Simon Pope, Rafael Artuch, Simon Heales, Shamima Rahman
Cerebral folate deficiency: Analytical tests and differential diagnosis. Journal of inherited metabolic disease 42 (4) (2019)
Nandaki Keshavan, Jose Abdenur, Glenn Anderson, Zahra Assouline, Giulia Barcia, Lamia Bouhikbar, Anupam Chakrapani, Maureen Cleary, Marta C Cohen, François Feillet, Carl Fratter, Natalie S Hauser, Tom Jacques, Amanda Lam, Helen McCullagh, Rahul Phadke, Agnès Rötig, Mark Sharrard, Mariella T Simon, Conrad Smith, Ewen W Sommerville, Robert W Taylor, Wyatt W Yue, Shamima Rahman
The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiency. Genetics in medicine : official journal of the American College of Medical Genetics 22 (1) (2019)
Bridget E Bax, Michelle Levene, Murray D Bain, Lynette D Fairbanks, Massimiliano Mirabella, Sema Kalkan Uçar, Thomas Klopstock, Cornelia Kornblum, Hanna Mandel, Shamima Rahman, Agathe Roubertie, Mauro Scarpelli, Philip M Sedgwick, Moshe Baru, Marcia Sellos-Moura, Jeanie Price, Patrick Horn, Niranjanan Nirmalananthan
Erythrocyte Encapsulated Thymidine Phosphorylase for the Treatment of Patients with Mitochondrial Neurogastrointestinal Encephalomyopathy: Study Protocol for a Multi-Centre, Multiple Dose, Open Label Trial. Journal of clinical medicine 8 (8) (2019)
Shanti Balasubramaniam, John Chrisodoulou, Shamima Rahman
Disorders of riboflavin metabolism. Journal of inherited metabolic disease 42 (4) (2019)
James E Davison, Shamima Rahman
Recognition, investigation and management of mitochondrial disease. Archives of disease in childhood 102 (11) (2017)

Shamima Rahman (S Rahman)

Publication Activity (10 Years)

Top Topics

Top Venues