222 results on '"Hussain, Nahin"'
Search Results
2. Safety and efficacy of tamoxifen in boys with Duchenne muscular dystrophy (TAMDMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
3. Approach to the pre-school child with sudden loss of consciousness
4. Safety and efficacy of tamoxifen in boys with Duchenne muscular dystrophy (TAMDMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
5. Diagnosis, assessment and management of nystagmus in childhood
6. Facial dysmorphism, hirsutism, and failure to thrive as manifestation of Leigh syndrome in a child with SURF1 mutation
7. 0900 Swirls and bright lights
8. Approach to a child with excessive daytime sleepiness
9. Phenotypical variation with same genetic mutation in familial hypokalemic periodic paralysis
10. Neuropsychological difficulties associated with dopa responsive dystonia
11. The SANAD II study of the effectiveness and cost-effectiveness of valproate versus levetiracetam for newly diagnosed generalised and unclassifiable epilepsy: an open-label, non-inferiority, multicentre, phase 4, randomised controlled trial
12. Case Report of 3-Phosphoglycerate Dehydrogenase Deficiency: A Baby with Severe Microcephaly, Psychomotor Delay, and Seizures
13. The SANAD II study of the effectiveness and cost-effectiveness of levetiracetam, zonisamide, or lamotrigine for newly diagnosed focal epilepsy: an open-label, non-inferiority, multicentre, phase 4, randomised controlled trial
14. Life Threatening Complication of Sore Throat: Lemierre’s Syndrome
15. Carersʼ express positive views on the acceptability, efficacy and safety of buccal midazolam for paediatric status epilepticus
16. Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures
17. Neuroimaging in Menkes disease
18. Aetiology, course and outcome of children admitted to paediatric intensive care with convulsive status epilepticus: A retrospective 5-year review
19. Cerebral proliferative angiopathy: A rare form of vascular malformation
20. Vitamin B12 Deficiency: A Treatable Cause of Developmental Delay In Infancy
21. Transition of children with epilepsies to adult care
22. Evaluation of staring episodes in children
23. Question 2 Should phenytoin and carbamazepine be avoided in Asian populations with the HLA-B*1502 positive genetic variant?
24. Freyʼs syndrome: a masquerader of food allergy
25. A structured approach to the assessment of a floppy neonate
26. A rare paediatric case of Klippel-Trenaunay- Weber syndrome
27. Voltage gated potassium channel antibodies positive autoimmune encephalopathy in a child: A case report and literature review of an under-recognized condition
28. Ambulatory electroencephalogram in children: A prospective clinical audit of 100 cases
29. Acute longitudinal myelitis as the first presentation in child with systemic lupus erythematosus
30. Phenotypic heterogeneity in skeletal muscle sodium channelopathies: a case report and literature review
31. Atypical juvenile neuronal ceroid lipofuscinosis: a report of three cases
32. Demyelination presenting as tics in a healthy child
33. Vitamin D deficiency in children with epilepsy: Do we need to detect and treat it?
34. Novel CLN1 mutation with atypical juvenile neuronal ceroid lipofuscinosis
35. MICrocephaly, disproportionate pontine and cerebellar hypoplasia syndrome: A clinico-radiologic phenotype linked to calcium/calmodulin-dependent serine protein kinase gene mutation
36. Globus pallidus high-signal lesions: A predominant MRI finding in children with neurofibromatosis type 1
37. Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial
38. Fifteen-minute consultation: an approach to a child presenting to the emergency department with acute psychotic symptoms
39. Bilateral thoracic outlet syndrome: An uncommon presentation of a rare condition in children
40. A rare cause of congenital ptosis: Blepharophimosis, ptosis and epicanthus inversus syndrome
41. Multiple cerebral cavernous haemangiomas in an infant
42. Acute disseminated encephalomyelitis presenting as pyrexia of unknown origin
43. A reminder of the dangers of trampolining: Spinal cord infarction secondary to hyperextension injury during trampolining
44. Severe anemia causing cerebral venous sinus thrombosis in an infant
45. Bulbar dysfunction: An early presentation of congenital myasthenic syndrome in three infants
46. Connatal Pelizaeus-Merzbacher disease: A great masquerader
47. peac (cyanotic expiratory apnoea of central origin) in Arnold Chiari II malformation
48. Question 2: Should thrombolytic agents be used in children presenting with acute ischaemic stroke?
49. Prolonged expiratory apnoea with cyanosis in Arnold Chiari II malformation
50. Fifteen-minute consultation: an approach to a child presenting to the emergency department with acute psychotic symptoms.
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