Diagnosis and treatment evaluation in patients with spontaneous intracranial hypotension

por Mehta, Dwij, Cheema, Sanjay, Davagnanam, Indran, Matharu, Manjit
Publicado 2023

When the penny drops

por Parkinson, Michael H, Patel, Rayna, Davagnanam, Indran, Wood, Nicholas W, Giunti, Paola
Publicado 2014

Pisa syndrome in Parkinson's disease: a mobile or fixed deformity?

por Doherty, Karen M, Davagnanam, Indran, Molloy, Sean, Silveira-Moriyama, Laura, Lees, Andrew J
Publicado 2013

Lymphomatosis cerebri: a treatable cause of rapidly progressive dementia

por Samani, Amit, Davagnanam, Indran, Cockerell, Oliver Charles, Ramsay, Alan, Patani, Rickie, Chataway, Jeremy
Publicado 2015

High b-value diffusion-weighted imaging in progressive multifocal leukoencephalopathy in HIV patients

por Godi, Claudia, De Vita, Enrico, Tombetti, Enrico, Davagnanam, Indran, Haddow, Lewis, Jäger, Hans Rolf
Publicado 2017

Trigeminal neurovascular contact in SUNCT and SUNA: a cross-sectional magnetic resonance study

por Lambru, Giorgio, Rantell, Khadija, O’Connor, Emer, Levy, Andrew, Davagnanam, Indran, Zrinzo, Ludvic, Matharu, Manjit
Publicado 2020

Visual Function and Brief Cognitive Assessment for Multiple Sclerosis in Optic Neuritis Clinically Isolated Syndrome Patients

por Collorone, Sara, Kanber, Baris, Hashem, Leen, Cawley, Niamh, Prados, Ferran, Davagnanam, Indran, Barkhof, Frederik, Ciccarelli, Olga, Toosy, Ahmed
Publicado 2022

Trigeminal microvascular decompression for short-lasting unilateral neuralgiform headache attacks

por Lambru, Giorgio, Lagrata, Susie, Levy, Andrew, Cheema, Sanjay, Davagnanam, Indran, Rantell, Khadija, Kitchen, Neil, Zrinzo, Ludvic, Matharu, Manjit
Publicado 2022

Is pituitary MRI screening necessary in cluster headache?

por Grangeon, Lou, O’Connor, Emer, Danno, Daisuke, Ngoc, Thanh Mai Pham, Cheema, Sanjay, Tronvik, Erling, Davagnanam, Indran, Matharu, Manjit
Publicado 2021

Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations

por Thust, Steffi, Veneziano, Liana, Parkinson, Michael H., Bhatia, Kailash P., Mantuano, Elide, Gonzalez-Robles, Cristina, Davagnanam, Indran, Giunti, Paola
Publicado 2022

Clinical Presentation, Investigation Findings, and Treatment Outcomes of Spontaneous Intracranial Hypotension Syndrome: A Systematic Review and Meta-analysis

por D’Antona, Linda, Jaime Merchan, Melida Andrea, Vassiliou, Anna, Watkins, Laurence Dale, Davagnanam, Indran, Toma, Ahmed Kassem, Matharu, Manjit Singh
Publicado 2021

Effect of white-matter lesions on the risk of periprocedural stroke after carotid artery stenting versus endarterectomy in the International Carotid Stenting Study (ICSS): a prespe...

por Ederle, Jörg, Davagnanam, Indran, van der Worp, H Bart, Venables, Graham S, Lyrer, Philippe A, Featherstone, Roland L, Brown, Martin M, Jäger, H Rolf
Publicado 2013

Brainstem phenotype of cathepsin A–related arteriopathy with strokes and leukoencephalopathy

por Hwang, Yun Tae, Lakshmanan, Rahul, Davagnanam, Indran, Thompson, Andrew G.B., Lynch, David S., Houlden, Henry, Bajaj, Nin, Eriksson, Sofia H., Bamiou, Doris-Eva, Warren, Jason D.
Publicado 2017

A model for interrogating the clinico‐radiological paradox in multiple sclerosis: Internuclear ophthalmoplegia

por Nij Bijvank, Jenny A., Sánchez Aliaga, Esther, Balk, Lisanne J., Coric, Danko, Davagnanam, Indran, Tan, H. Stevie, Uitdehaag, Bernard M. J., van Rijn, Laurentius J., Petzold, Axel
Publicado 2021

Redefining the phenotype of ALSP and AARS2 mutation–related leukodystrophy

por Lakshmanan, Rahul, Adams, Matthew E., Lynch, David S., Kinsella, Justin A., Phadke, Rahul, Schott, Jonathan M., Murphy, Elaine, Rohrer, Jonathan D., Chataway, Jeremy, Houlden, Henry, Fox, Nick C., Davagnanam, Indran
Publicado 2017

Brain microstructural and metabolic alterations detected in vivo at onset of the first demyelinating event

por Collorone, Sara, Prados, Ferran, Kanber, Baris, Cawley, Niamh M, Tur, Carmen, Grussu, Francesco, Solanky, Bhavana S, Yiannakas, Marios, Davagnanam, Indran, Wheeler-Kingshott, Claudia A M Gandini, Barkhof, Frederik, Ciccarelli, Olga, Toosy, Ahmed T
Publicado 2021

Extra-ocular muscle MRI in genetically-defined mitochondrial disease

por Pitceathly, Robert D. S., Morrow, Jasper M., Sinclair, Christopher D. J., Woodward, Cathy, Sweeney, Mary G., Rahman, Shamima, Plant, Gordon T., Ali, Nadeem, Bremner, Fion, Davagnanam, Indran, Yousry, Tarek A., Hanna, Michael G., Thornton, John S.
Publicado 2015

ANGPTL6 Genetic Variants Are an Underlying Cause of Familial Intracranial Aneurysms

por Hostettler, Isabel C., O'Callaghan, Benjamin, Bugiardini, Enrico, O'Connor, Emer, Vandrovcova, Jana, Davagnanam, Indran, Alg, Varinder, Bonner, Stephen, Walsh, Daniel, Bulters, Diederik, Kitchen, Neil, Brown, Martin M., Grieve, Joan, Werring, David J., Houlden, Henry
Publicado 2021

Survey of healthcare professionals’ knowledge, attitudes and practices regarding spontaneous intracranial hypotension

por Cheema, Sanjay, Anderson, Jane, Duncan, Callum, Davagnanam, Indran, Armstrong, Paul, Redfern, Nancy, Ordman, Anthony, D’Antona, Linda, Nissen, Justin, Sayal, Parag, Vaughan-Huxley, Eyston, Lagrata, Susie, Iodice, Valeria, Snape-Burns, Jessica, Joy, Clare, Matharu, Manjit
Publicado 2022

Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination

por Chelban, Viorica, Patel, Nisha, Vandrovcova, Jana, Zanetti, M. Natalia, Lynch, David S., Ryten, Mina, Botía, Juan A., Bello, Oscar, Tribollet, Eloise, Efthymiou, Stephanie, Davagnanam, Indran, Bashiri, Fahad A., Wood, Nicholas W., Rothman, James E., Alkuraya, Fowzan S., Houlden, Henry
Publicado 2017