Clinical presentation and prognosis in MOG-antibody disease: a UK study von Jurynczyk, Maciej, Messina, Silvia, Woodhall, Mark R, Raza, Naheed, Everett, Rosie, Roca-Fernandez, Adriana, Tackley, George, Hamid, Shahd, Sheard, Angela, Reynolds, Gavin, Chandratre, Saleel, Hemingway, Cheryl, Jacob, Anu, Vincent, Angela, Leite, M Isabel, Waters, Patrick, Palace, Jacqueline

Volltext

Distinct brain imaging characteristics of autoantibody-mediated CNS conditions and multiple sclerosis von Jurynczyk, Maciej, Geraldes, Ruth, Probert, Fay, Woodhall, Mark R, Waters, Patrick, Tackley, George, DeLuca, Gabriele, Chandratre, Saleel, Leite, Maria I, Vincent, Angela, Palace, Jacqueline

Volltext

Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series von Taylor, John, Craft, Jude, Blair, Edward, Wordsworth, Sarah, Beeson, David, Chandratre, Saleel, Cossins, Judith, Lester, Tracy, Németh, Andrea H, Ormondroyd, Elizabeth, Patel, Smita Y, Pagnamenta, Alistair T, Taylor, Jenny C, Thomson, Kate L, Watkins, Hugh, Wilkie, Andrew O M, Knight, Julian C

Volltext

Endocrinopathies in paediatric-onset neuromyelitis optica spectrum disorder with aquaporin 4 (AQP4) antibody von Hacohen, Yael, Messina, Silvia, Gan, Hoong-Wei, Wright, Sukhvir, Chandratre, Saleel, Leite, Maria Isabel, Fallon, Penny, Vincent, Angela, Ciccarelli, Olga, Wassmer, Evangeline, Lim, Ming, Palace, Jacqueline, Hemingway, Cheryl

Volltext

Neuromyelitis Optica Spectrum Disorders With Aquaporin-4 and Myelin-Oligodendrocyte Glycoprotein Antibodies: A Comparative Study von Kitley, Joanna, Waters, Patrick, Woodhall, Mark, Leite, M. Isabel, Murchison, Andrew, George, Jithin, Küker, Wilhelm, Chandratre, Saleel, Vincent, Angela, Palace, Jacqueline

Volltext

A phase 3 randomized placebo-controlled trial of tadalafil for Duchenne muscular dystrophy von Victor, Ronald G, Sweeney, H Lee, Finkel, Richard, McDonald, Craig M, Byrne, Barry, Eagle, Michelle, Goemans, Nathalie, Vandenborne, Krista, Dubrovsky, Alberto L, Topaloglu, Haluk, Miceli, M Carrie, Furlong, Pat, Landry, John, Elashoff, Robert, Cox, David

Volltext

Trends in phenotype in the English paediatric neurofibromatosis type 2 cohort stratified by genetic severity von Halliday, Dorothy, Emmanouil, Beatrice, Vassallo, Grace, Lascelles, Karine, Nicholson, James, Chandratre, Saleel, Anand, Geetha, Wasik, Martin, Pretorius, Pieter, Evans, D. Gareth, Parry, Allyson, Axon, Patrick, Gair, Juliette, Smyth, Carolyn, Afridi, Shazia K, Obholzer, Rupert, Everett, Vanessa, Jarvis, Nicola, Henshaw, Kirsty, Hanemann, C Oliver, Howard, Wendy, May, Anne, Redman, Carolyn, Rattihalli, Rohini, Tomkins, Helen

Volltext

Trends in phenotype in the English paediatric Neurofibromatosis Type 2 cohort stratified by genetic severity von Halliday, Dorothy, Emmanouil, Beatrice, Vassallo, Grace, Lascelles, Karine, Nicholson, James, Chandratre, Saleel, Anand, Geetha, Wasik, Martin, Pretorius, Pieter, Evans, D Gareth

Volltext

H1N1 triggered recurrent acute necrotizing encephalopathy in a family with a T653I mutation in the RANBP2 gene von Anand, Geetha, Visagan, Ravindran, Chandratre, Saleel, Segal, Shelley, Nemeth, Andrea H, Squier, Waney, Sheerin, Fintan, Neilson, Derek, Jayawant, Sandeep

Volltext

Avoiding Premature Diagnostic Closure: Lessons from Two Children with Neurotransmitter Disorders Associated with Dual Pathology von Salazar‐Villacorta, Ainara, Spaull, Robert, Chowdhury, Samyami, Mukhtyar, Bina, Chitre, Manali, Armstrong, Ruth, Sa, Mario, Chandratre, Saleel, Kini, Usha, Chinthapalli, Ravi, Mankad, Kshitij, Sudhakar, Sniya, Pope, Simon, Heales, Simon, Kurian, Manju A.

Volltext

Familial idiopathic intracranial hypertension with variable phenotype von Beri, Sushil, Chandratre, Saleel, Chow, Gabriel

Volltext

Neuromyelitis optica relapses: Race and rate, immunosuppression and Impairment von Tackley, George, O’Brien, Fanny, Rocha, João, Woodhall, Mark, Waters, Patrick, Chandratre, Saleel, Halfpenny, Christopher, Hemingway, Cheryl, Wassmer, Evangeline, Wasiewski, Warren, Leite, Maria Isabel, Palace, Jacqueline

Volltext

Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond von Elbashir, Haitham, Fathalla, Waseem, Mundada, Vivek, Iqbal, Mehtab, Al Tawari, Asmaa A, Chandratre, Saleel, Bastaki, Laila, Romany, Ingy, Ismayl, Omar, Abou Tayoun, Ahmad

Volltext

Endocrinopathies in paediatric-onset Aquaporin 4 (AQP4) antibody neuromyelitis optica spectrum disorder von Hacohen, Yael, Messina, Silvia, Gan, Hoong-Wei, Wright, Sukhvir, Chandratre, Saleel, Leite, Maria Isabel, Fallon, Penny, Vincent, Angela, Ciccarelli, Olga, Wassmer, Evangeline, Lim, Ming, Palace, Jacqueline, Hemingway, Cheryl

Volltext

Avoiding Premature Diagnostic Closure: Lessons from Two Children with Neurotransmitter Disorders Associated with Dual Pathology von Salazar‐Villacorta, Ainara, Spaull, Robert, Chowdhury, Samyami, Mukhtyar, Bina, Chitre, Manali, Armstrong, Ruth, Sa, Mario, Chandratre, Saleel, Kini, Usha, Chinthapalli, Ravi, Mankad, Kshitij, Sudhakar, Sniya, Pope, Simon, Heales, Simon, Kurian, Manju A

Volltext bestellen

Additional file 1: of Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series von Taylor, John, Craft, Jude, Blair, Edward, Wordsworth, Sarah, Beeson, David, Saleel Chandratre, Cossins, Judith, Lester, Tracy, Németh, Andrea, Ormondroyd, Elizabeth, Patel, Smita, Pagnamenta, Alistair, Taylor, Jenny, Thomson, Kate, Watkins, Hugh, Wilkie, Andrew, Knight, Julian

Volltext bestellen