J. Wilmshurst

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RYR1 mutations are a common cause of congenital myopathies with central nuclei

Straub, F. Muntoni, S. Al-Sarraj, 2010, Annals of neurology.

Accelerated Immunodeficiency-associated Vaccine-derived Poliovirus Serotype 3 Sequence Evolution Rate in an 11-week-old Boy With X-linked Agammaglobulinemia and Perinatal Human Immunodeficiency Virus Exposure

Y. Lau, B. Eley, J. Wilmshurst, 2019, Clinical Infectious Diseases.

Management of Children with Status Epilepticus

J. Wilmshurst, 2015 .

Epidemiology of children with epilepsy at a tertiary referral centre in South Africa

J. Wilmshurst, S. Ackermann, S. L. Roux, 2019, Seizure.

Epileptic spasms — 175 years on: Trying to teach an old dog new tricks

J. Wilmshurst, F. O'callaghan, R. Ibekwe, 2017, Seizure.

RyR1 Deficiency in Congenital Myopathies Disrupts Excitation–Contraction Coupling

F. Muntoni, M. Duchen, K. Mamchaoui, 2013, Human mutation.

Characteristics and outcome of children with juvenile dermatomyositis in Cape Town: a cross-sectional study

J. Wilmshurst, M. Esser, C. Scott, 2016, Pediatric Rheumatology.

Medical cannabis: What practitioners need to know.

J. Wilmshurst, M. Blockman, M. Blockman, 2020, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Withdrawal of parenteral phenobarbitone--implications for resource-poor countries.

J. Wilmshurst, C. Newton, R. van Toorn, 2005, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Analysis of a Subacute Sclerosing Panencephalitis Genotype B3 Virus from the 2009-2010 South African Measles Epidemic Shows That Hyperfusogenic F Proteins Contribute to Measles Virus Infection in the Brain

B. Eley, M. Porotto, A. Moscona, 2018, Journal of Virology.

Moyamoya Syndrome in South African Children With HIV-1 Infection

N. Wieselthaler, B. Eley, R. Govender, 2016, Journal of child neurology.

Clinical characteristics of children with epilepsy managed at an urban hospital in Africa: a retrospective study

K. Donald, J. Wilmshurst, C. Newton, 2019, Journal of the International Child Neurology Association.

Bridging the childhood epilepsy treatment gap in northern Nigeria (BRIDGE): Rationale and design of pre-clinical trial studies

Aminu T. Abdullahi, P. Carney, M. DeBaun, 2019, Contemporary clinical trials communications.

Prevalence of Seizures in Children Infected With Human Immunodeficiency Virus

B. Eley, J. Wilmshurst, P. Samia, 2013, Journal of child neurology.

Child Neurology Services in Africa

J. Wilmshurst, C. Newton, M. Mallewa, 2011, Journal of child neurology.

The role of ICNA in Africa

H. Chugani, J. Wilmshurst, C. Newton, 2011, Developmental medicine and child neurology.

RRTM_A_201159 91..102

J. Wilmshurst, C. Newton, S. Kariuki, 2019 .

Epilepsy diagnosis and management of children in Kenya: review of current literature

J. Wilmshurst, C. Newton, S. Kariuki, 2019, Research and reports in tropical medicine.

Neuropsychiatric and Neurocognitive Manifestations in HIV-Infected Children Treated With Efavirenz in South Africa—A Retrospective Case Series

B. Eley, J. Wilmshurst, C. Hammond, 2019, Front. Neurol..

Overnight oximetry in African children with human immunodeficiency virus

F. Kirkham, B. Eley, N. Dlamini, 2012, Archives of Disease in Childhood.

Peripheral neuropathies of childhood

J. Wilmshurst, 2009 .

Common Childhood Epilepsy Mimics

J. Wilmshurst, P. Samia, 2020 .

Keeping people with epilepsy safe during the COVID-19 pandemic

Josemir W Sander, I. Scheffer, M. Brodie, 2020, Neurology.

Why does Africa have the lowest number of Neurologists and how to cover the Gap?

J. Wilmshurst, N. Kissani, P. Mbelesso, 2021, Journal of the Neurological Sciences.

Precision medicine for developmental and epileptic encephalopathies in Africa: strategies for a resource-limited setting.

Jeffrey M. Weiss, G. Carvill, H. Mefford, 2022, medRxiv.

Vitamin D abnormalities and bone turn over analysis in children with Epilepsy in the Western Cape of South Africa

J. Wilmshurst, B. Gidal, G. Watt, 2019, Seizure.

Vitamin D abnormalities and bone turn over analysis in children with epilepsy in the Western Cape of South Africa.

J. Wilmshurst, B. Gidal, G. Watt, 2019, Seizure.

Rapid onset transverse myelitis in adolescence: implications for pathogenesis and prognosis

M. Walker, J. Wilmshurst, K. Pohl, 1999, Archives of disease in childhood.

Hereditary peripheral neuropathies of childhood: An overview for clinicians

J. Wilmshurst, R. Ouvrier, 2011, Neuromuscular Disorders.

Peripheral neuropathies of infancy.

J. Pollard, G. Nicholson, J. Wilmshurst, 2003, Developmental medicine and child neurology.

Severe infantile axonal neuropathy with respiratory failure

A. Bye, J. Pollard, J. Wilmshurst, 2001, Muscle & nerve.

Neurologic and Neurobehavioral Sequelae in Children With Human Immunodeficiency Virus (HIV-1) Infection

B. Eley, R. Govender, J. Wilmshurst, 2011, Journal of child neurology.

Systematic review of the screening, diagnosis, and management of ADHD in children with epilepsy. Consensus paper of the Task Force on Comorbidities of the ILAE Pediatric Commission

E. Wirrell, L. Carmant, B. Hermann, 2018, Epilepsia.

Utility of genetic testing in children with developmental and epileptic encephalopathy (DEE) at a tertiary hospital in South Africa: A prospective study

Shahida Moosa, J. Wilmshurst, R. Solomons, 2022, Seizure.

Pediatric Status Epilepticus

J. Wilmshurst, M. Mekki, R. Ibekwe, 2020, Clinical Child Neurology.

Progressive multifocal leukoencephalopathy after initiation of highly active antiretroviral therapy in a child with advanced human immunodeficiency virus infection: a case of immune reconstitution inflammatory syndrome.

B. Eley, G. Hussey, J. Wilmshurst, 2004, The Pediatric infectious disease journal.

The assessment and management of pain in children with Guillain-Barré Syndrome in a sub-Saharan setting.

J. Wilmshurst, Hayley Hutton, 2019 .

Subacute sclerosing panencephalitis: clinical phenotype, epidemiology, and preventive interventions

B. Eley, J. Wilmshurst, D. Hardie, 2019, Developmental medicine and child neurology.

Diagnosis and management of pediatric peripheral neuropathies in resource-poor settings

J. Wilmshurst, 2013 .

Markers of susceptibility to acute rheumatic fever: the B-cell antigen D8/17 is not robust as a marker in South Africa

J. Wilmshurst, J. Lawrenson, J. Hughes, 2011, Cardiology in the Young.

Neuropathies Secondary to Systemic Disorders

J. Wilmshurst, R. Ouvrier, 2015 .

Cerebrovascular disease in children with HIV‐1 infection

N. Wieselthaler, B. Eley, J. Wilmshurst, 2016, Developmental medicine and child neurology.

Position Statement:Emerging genetic therapies for rare disorders

A. Kirton, I. Tein, H. Topaloglu, 2019, Journal of the International Child Neurology Association.

NeuroAIDS in children.

B. Eley, J. Wilmshurst, K. Cohen, 2018, Handbook of clinical neurology.

Overview of the Effect and Epidemiology of Parasitic Central Nervous System Infections in African Children

J. Wilmshurst, M. Mallewa, 2014, Seminars in pediatric neurology.

Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go

M. Schroth, D. Zafeiriou, Y. Chien, 2021, Neuromuscular Disorders.

Management of mental health disorders and central nervous system sequelae in HIV-positive children and adolescents

B. Eley, K. Donald, B. Moos, 2014 .

Clearance of Immunodeficiency-associated Vaccine-derived Poliovirus Infection With Pocapavir.

B. Eley, J. Wilmshurst, M. Collett, 2020, The Pediatric infectious disease journal.

Stroke transcranial Doppler in children with human immunodeficiency virus

F. Kirkham, B. Eley, N. Dlamini, 2020, Developmental medicine and child neurology.

Peripheral nerve disease secondary to systemic conditions in children.

M. Ryan, J. Wilmshurst, R. Ouvrier, 2019, Therapeutic advances in neurological disorders.

Clinical Phenotype of South African Children With Neurofibromatosis 1

K. Fieggen, C. Adnams, J. Wilmshurst, 2006, Journal of child neurology.

Spinal muscular atrophy in black South Africans: concordance with the universal SMN1 genotype

J. Wilmshurst, F. Leisegang, H. Henderson, 2002, Clinical genetics.

Duchenne muscular dystrophy: High-resolution melting curve analysis as an affordable diagnostic mutation scanning tool in a South African cohort.

R. Goliath, J. Wilmshurst, A. Esterhuizen, 2014, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Intellectual and Behavioral Functioning in a South African Cohort of Boys With Duchenne Muscular Dystrophy

K. Thomas, K. Donald, J. Wilmshurst, 2011, Journal of child neurology.

Specific Neurologic Complications of Human Immunodeficiency Virus Type 1 (HIV-1) Infection in Children

B. Eley, J. Wilmshurst, P. Hartley, 2006, Journal of child neurology.

Duchenne muscular dystrophy in the Western Cape, South Africa: Where do we come from and where are we going?

R. Goliath, J. Wilmshurst, A. Esterhuizen, 2016, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

A case for genomic medicine in South African paediatric patients with neuromuscular disease

S. Bardien, M. Schoonen, F. H. van der Westhuizen, 2022, Frontiers in Pediatrics.

Use of phenobarbitone for treating childhood epilepsy in resource-poor countries.

J. Wilmshurst, R. van Toorn, 2005, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Seizures in Children with HIV infection in South Africa: A retrospective case control study

K. Donald, J. Wilmshurst, R. Burman, 2019, Seizure.

Clinical characteristics of children with epilepsy managed at a tertiary hospital in Africa: a retrospective study

K. Donald, J. Wilmshurst, C. Newton, 2019 .

An overview of the effect and epidemiology of viral central nervous system infections in African children.

J. Wilmshurst, E. Badoe, 2014, Seminars in pediatric neurology.

The challenges and innovations for therapy in children with epilepsy

L. Lagae, A. Berg, J. Wilmshurst, 2014, Nature Reviews Neurology.

Summary of recommendations for the management of infantile seizures: Task Force Report for the ILAE Commission of Pediatrics

E. Mizrahi, D. Hirtz, W. Gaillard, 2015, Epilepsia.

Definitive neuroradiological diagnostic features of tuberculous meningitis in children

Savvas Andronikou, S. Andronikou, H. Douis, 2004, Pediatric Radiology.

Giant Congenital Melanocytic Nevi in a Patient With Brain Structural Malformations and Multiple Lipomatosis

N. Wieselthaler, J. Wilmshurst, R. van Toorn, 2002, Journal of child neurology.

Clinical characteristics and neurodevelopmental outcomes of children with tuberculous meningitis and hydrocephalus

A. Figaji, J. Wilmshurst, L. Padayachy, 2016, Developmental medicine and child neurology.

The Diagnostic Difficulties of Complex Glycerol Kinase Deficiency

J. Wilmshurst, Veruschka Ramanjam, S. Delport, 2010, Journal of child neurology.

Neuropsychiatric complications of efavirenz in children with HIV infection

B. Eley, J. Wilmshurst, C. Hammond, 2016 .

Neurologic complications of pediatric human immunodeficiency virus: implications for clinical practice and management challenges in the African setting.

B. Eley, K. Donald, J. Wilmshurst, 2014, Seminars in pediatric neurology.

A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance

G. Ravenscroft, N. Laing, J. Wilmshurst, 2011, Neuromuscular Disorders.

Epigenetic changes as a common trigger of muscle weakness in congenital myopathies.

F. Muntoni, R. Gambari, A. Finotti, 2015, Human molecular genetics.

HIV Encephalopathy: pediatric case series description and insights from the clinic coalface

B. Eley, K. Donald, N. Langerak, 2015, AIDS Research and Therapy.

Update on the key developments of the neurologic complications in children infected with HIV

B. Eley, K. Donald, J. Wilmshurst, 2014, Current opinion in HIV and AIDS.

Clinical Application of Epilepsy Genetics in Africa: Is Now the Time?

G. Carvill, R. Ramesar, A. Poduri, 2018, Front. Neurol..

Acquired Demyelinating Disorders of Childhood in the Western Cape, South Africa

N. Wieselthaler, R. Govender, J. Wilmshurst, 2010, Journal of child neurology.

Skin cells for use in an alternate diagnostic method for Duchenne muscular dystrophy

J. Wilmshurst, L. Tyers, L. Davids, 2018, Neuromuscular Disorders.

The First Case of Riboflavin Transporter Deficiency in sub-Saharan Africa.

F. H. van der Westhuizen, K. Fieggen, M. Menezes, 2017, Seminars in pediatric neurology.

Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1

T. Wienker, E. Bertini, A. Pfeufer, 2001, Nature Genetics.

Dravet syndrome in South African infants: Tools for an early diagnosis

G. Carvill, H. Mefford, R. Ramesar, 2018, Seizure.

Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study

M. Jaatun, K. Katanyuwong, P. Kwan, 2018, Epilepsia open.

Post-Infectious Autoimmunity in the Central (CNS) and Peripheral (PNS) Nervous Systems: An African Perspective

B. Eley, A. Vincent, H. Willison, 2022, Frontiers in Immunology.

Hydatid Disease of the Spine in South African Children

J. Wilmshurst, A. Ndondo, G. Fieggen, 2003, Journal of child neurology.

Distribution of brain infarction in children with tuberculous meningitis and correlation with outcome score at 6 months

S. Andronikou, M. Hatherill, J. Wilmshurst, 2006, Pediatric Radiology.

Position statement by the ICNA in Support of vaccinating all children against measles virus

J. Wilmshurst, R. Idro, P. Samia, 2020, Journal of the International Child Neurology Association.

Objective CT criteria to determine the presence of abnormal basal enhancement in children with suspected tuberculous meningitis

S. Andronikou, J. Wilmshurst, S. Przybojewski, 2006, Pediatric Radiology.

Value of early follow-up CT in paediatric tuberculous meningitis

S. Andronikou, N. Wieselthaler, A. G. Fieggen, 2005, Pediatric Radiology.

Peripheral neuropathies of infancy

J. Pollard, G. Nicholson, J. Wilmshurst, 2003 .

The African Pediatric Fellowship Program: Training in Africa for Africans

H. Zar, J. Wilmshurst, N. Kennedy, 2016, Pediatrics.

Threats to the child’s brain in resource-poor countries

J. Wilmshurst, 2017 .

The characteristics of juvenile myasthenia gravis among South Africans.

J. Wilmshurst, J. Heckmann, R. van Toorn, 2012, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Presentation and outcome of sacral agenesis: 20 years' experience

J. Wilmshurst, M. Borzyskowski, R. Kelly, 1999, Developmental medicine and child neurology.

Positron Emission Tomography in Imaging Spinal Cord Tumors

T. Cox, S. Barrington, J. Wilmshurst, 2000, Journal of child neurology.

Hemiatrophy of the Spinal Cord in a Patient With Mucopolysaccharidosis Type IIIB

N. Wieselthaler, J. Wilmshurst, P. Samia, 2010, Journal of child neurology.

Acquired Demyelinating Disorders of the CNS in Children

N. Wieselthaler, R. Govender, J. Wilmshurst, 2012 .

An update on the treatment of Sydenham’s chorea: the evidence for established and evolving interventions

J. Wilmshurst, K. Walker, 2010, Therapeutic advances in neurological disorders.

Sydenham's chorea--clinical and therapeutic update 320 years down the line.

J. Wilmshurst, J. Lawrenson, K. Walker, 2006, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Treatment of Sydenham Chorea With Intravenous Immunoglobulin

J. Wilmshurst, J. Lawrenson, A. Brink, 2012, Journal of child neurology.

Sydenham Chorea and PANDAS in South Africa

Dan J Stein, P. D. de Vries, J. Wilmshurst, 2015, Journal of child neurology.

Neuropsychiatric movement disorders following streptococcal infection.

J. Wilmshurst, J. Lawrenson, K. Walker, 2005, Developmental medicine and child neurology.

Neuropsychiatric movement disorders following streptococcal infection

J. Wilmshurst, J. Lawrenson, K. Walker, 2005 .

Children With Epilepsy in Africa

Charles R. Newton, H. Chugani, D. Hirtz, 2013, Journal of child neurology.

Congenital Cervical Spinal Cord Lesions: Pathogenesis, Management, and Outcome

N. Wieselthaler, R. Govender, J. Wilmshurst, 2007, Journal of child neurology.

Autism Spectrum Disorders in Africa: Current Challenges in Identification, Assessment, and Treatment

D. Skuse, H. Chugani, D. Chugani, 2016, Journal of child neurology.

Autism Spectrum Disorders in Africa : Current Challenges in Identification , Assessment , and Treatment : A Report on the International Child Neurology Association Meeting on ASD in Af

Diane C. Chugani, Harry T. Chugani, Kirsten A. Donald, 2016 .

A qualitative study exploring caregivers’ experiences, perspectives, and expectations for precision medicine in epilepsy in South Africa

K. Fieggen, J. Wilmshurst, N. Laing, 2021, Epilepsy & Behavior.

Parental Understanding of Tuberous Sclerosis Complex

K. Donald, J. Wilmshurst, P. Samia, 2015, Journal of child neurology.

Epilepsy is ubiquitous, but more devastating in the poorer regions of the world… or is it?

G. Birbeck, J. Wilmshurst, C. Newton, 2014, Epilepsia.

Gillespie Syndrome: Two Further Cases

K. Donald, J. Wilmshurst, A. Crutchley, 2006, Journal of child neurology.

Neuropsychological manifestations in children with Sydenham’s chorea after adjunct intravenous immunoglobulin and standard treatment

S. Seedat, C. Lochner, J. Wilmshurst, 2016, Metabolic Brain Disease.

Subacute sclerosing panencephalitis in South African children following the measles outbreak between 2009 and 2011.

B. Eley, J. Wilmshurst, A. Ndondo, 2015, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

A Comparison of Parenteral Phenobarbital vs. Parenteral Phenytoin as Second-Line Management for Pediatric Convulsive Status Epilepticus in a Resource-Limited Setting

J. Wilmshurst, A. Ndondo, S. Ackermann, 2019, Front. Neurol..

The Usefulness of Electroencephalograms in a Survey of Children From the Western Cape of South Africa

J. Wilmshurst, G. Riordan, K. Donald, 2012, Journal of child neurology.

Two unusual causes of pituitary stalk thickening in children without clinical features of diabetes insipidus

S. Andronikou, A. G. Fieggen, J. Wilmshurst, 2003, Pediatric Radiology.

Advocacy for children with epilepsy: Leveraging the WHA resolution. Advocacy Task Force, Commission of Pediatrics, International League Against Epilepsy

A. Guekht, E. Perucca, J. Helen Cross, 2018, Epilepsia open.

Migrating Partial Seizures in Infancy: Two New Cases

J. Wilmshurst, D. B. Appleton, Padraic J. Grattan-Smith, 2000, Journal of child neurology.

The role of melatonin to attain electroencephalograms in children in a sub-Saharan African setting

J. Wilmshurst, R. Ibekwe, Lata Jeaven, 2017, Seizure.

Cerebellar ataxia, anterior horn cell disease, learning difficulties, and dystonia: a new syndrome.

R. Robinson, R. Surtees, J. Wilmshurst, 2000, Developmental medicine and child neurology.

Approach to a Child with Epilepsy

J. Wilmshurst, E. Kija, 2020 .

Diagnosis, monitoring and treatment of tuberous sclerosis complex: A South African consensus response to international guidelines

J. Wilmshurst, P. D. Vries, A. Venter, 2017 .

P115 – 2579: Clinical presentation of Tuberous Sclerosis Complex in Cape Town, South Africa

J. Wilmshurst, E. Kija, P. Samia, 2015 .

The challenges of managing children with epilepsy in Africa.

J. Wilmshurst, C. Newton, A. Kakooza-Mwesige, 2014, Seminars in pediatric neurology.

Chronic axonal neuropathy with triosephosphate isomerase deficiency.

J. Pollard, J. Wilmshurst, R. Ouvrier, 2004, Pediatric neurology.

Leaving the party -- withdrawal of South African essential medicines.

M. McCulloch, J. Wilmshurst, M. Blockman, 2006, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Pediatric Cerebral Palsy in Africa

H. Chugani, A. Majnemer, K. Donald, 2015, Journal of child neurology.

MRI findings in acute idiopathic transverse myelopathy in children

S. Andronikou, J. Wilmshurst, R. Hewlett, 2003, Pediatric Radiology.

Development of a Duchenne Muscular Dystrophy registry for children in South Africa to optimize care

J. Wilmshurst, A. Ndondo, A. Jalloh, 2019, Journal of the International Child Neurology Association.

A retrospective description of primary immuno-deficiency diseases at Red Cross War Memorial Children's Hospital, Cape Town, South Africa, 1975 - 2017.

B. Eley, M. Levin, J. Wilmshurst, 2020, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Neurologic Care of Forcibly Displaced Persons

Lyell K. Jones, G. Birbeck, Amy Bennett, 2023, Neurology.

Roadmap for a competency-based educational curriculum in epileptology : report of the Epilepsy Education Task Force of the International League Against Epilepsy

J. Gotman, I. Rektor, J. Wilmshurst, 2019 .

Epileptic spasms: Evidence for oral corticosteroids and implications for low and middle income countries

J. Wilmshurst, Sharika V. Raga, Jo M. Wilmshurst, 2018, Seizure.

Comorbidities Affecting Children with Epilepsy – Not a Novel Entity but New Insights Could Improve Holistic Care

J. Wilmshurst, Tandokazi Quvile, 2016 .

Importance of genetic diagnosis in the management of early-onset epilepsies.

G. Carvill, K. Fieggen, R. Ramesar, 2020, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegia

M. Benatar, M. Reilly, J. Wilmshurst, 2023, Frontiers in neurology.

HIV Encephalopathy: pediatric case series description and insights from the clinic coalface.

B. Eley, K. Donald, N. Langerak, 2015, AIDS research and therapy.

Spinal Muscular Atrophy With Congenital Fractures: Postmortem Analysis

J. Wilmshurst, R. van Toorn, J. Davies, 2002, Journal of child neurology.

Classification of Childhood Epileptic Seizures

J. Wilmshurst, C. Hammond, 2020 .

Precision medicine for developmental and epileptic encephalopathies in Africa-strategies for a resource-limited setting.

Karynne E. Patterson, G. Carvill, H. Mefford, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Vitamin D abnormalities and bone turn over analysis in children with epilepsy in the Western Cape of South Africa.

J. Wilmshurst, B. Gidal, G. Watt, 2019, Seizure.

The challenges of managing children with epilepsy in Africa.

J. Wilmshurst, C. Newton, A. Kakooza-Mwesige, 2014, Seminars in pediatric neurology.

Neurologic and Neurobehavioral Sequelae in Children With Human Immunodeficiency Virus (HIV-1) Infection

B. Eley, R. Govender, J. Wilmshurst, 2011, Journal of child neurology.

Familial Guillain—Barré Syndrome

R. Vaughan, R. Hughes, J. Wilmshurst, 1999, European journal of neurology.

Neuropsychological manifestations in children with Sydenham’s chorea after adjunct intravenous immunoglobulin and standard treatment

S. Seedat, C. Lochner, J. Wilmshurst, 2015, Metabolic Brain Disease.

Normal Outcome With Prenatal Intervention for Riboflavin Transporter Defect.

J. Wilmshurst, Sharika Raga, Natasha Elks, 2023, Pediatric neurology.

Tuberous sclerosis complex in the Western Cape, South Africa: The clinical presentation features.

J. Wilmshurst, E. Kija, P. Samia, 2017, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Cerebrovascular disease in children with HIV‐1 infection

N. Wieselthaler, B. Eley, J. Wilmshurst, 2016, Developmental medicine and child neurology.