Antonia Clarke

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Is chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS) in children the same condition as in adults?

T. Jacques, A. Childs, W. Chong, 2019, Developmental medicine and child neurology.

Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids ( CLIPPERS ) in children – a highly aggressive condition

T. Jacques, M. Lim, C. Hemingway, 2019 .

Genetic neuropathies presenting with CIDP-like features in childhood

P. Fallon, M. Kinali, H. Jungbluth, 2020, Neuromuscular Disorders.

Biallelic mutations in NRROS cause an early onset lethal microgliopathy

M. Nolan, B. McColl, Y. Crow, 2020, Acta Neuropathologica.

A new Nav1.7 sodium channel mutation I234T in a child with severe pain

C. Woods, S. Dib-Hajj, S. Waxman, 2010, European journal of pain.

Recurrent acute necrotizing encephalopathy following influenza A in a genetically predisposed family

P. Rich, D. Neilson, Sachin Gupta, 2010, Developmental medicine and child neurology.

Idiopathic catastrophic epileptic encephalopathy presenting with acute onset intractable status

B. Harding, R. Surtees, H. Cross, 2003, Seizure.

SURF1 deficiency: a multi-centre natural history study

Robert W. Taylor, E. Aasheim, S. Rahman, 2013, Orphanet Journal of Rare Diseases.

Biallelic DNAJC3 variants in a neuroendocrine developmental disorder with insulin dysregulation

I. C. Lloyd, D. Smedley, M. McEntagart, 2021, Clinical dysmorphology.

Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.

M. Adams, A. Fasano, A. Bassuk, 2009, American journal of human genetics.

Pediatric Herpes Simplex Virus Encephalitis Complicated by N-Methyl-D-aspartate Receptor Antibody Encephalitis.

A. Vincent, Jean-Pierre Lin, V. Sancho-Shimizu, 2015, Journal of the Pediatric Infectious Diseases Society.

Acute life threatening cerebellitis presenting with no apparent cerebellar signs

A. Siddiqui, M. Lim, Y. Hacohen, 2011, Clinical neurology and neurosurgery (Dutch-Flemish ed. Print).

Mutations in SCN4A: A Rare but Treatable Cause of Recurrent Life-Threatening Laryngospasm

M. Hanna, H. Jungbluth, S. V. Tan, 2014, Pediatrics.

Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigens

P. Fallon, H. Cross, A. Vincent, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

Acute flaccid weakness with myelopathy and peripheral nerve involvement in 2 children: Recent characterization of a previously observed phenomenon.

M. Lim, G. Olivé, K. Doerholt, 2016, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Autistic regression associated with seizure onset in an infant with tuberous sclerosis.

P. Bolton, A. Humphrey, B. Neville, 2006, Developmental medicine and child neurology.

GLUT-1 deficiency presenting with seizures and reversible leukoencephalopathy on MRI imaging.

F. Elmslie, Y. Hacohen, N. Ismayilova, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Progressive myoclonic epilepsy with Fanconi syndrome

E. Seaby, R. Pengelly, S. Ennis, 2016, JRSM open.