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January-April 2014
Volume 9 | Issue 1
Page Nos. 1-93

Online since Friday, April 25, 2014

Accessed 66,932 times.

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REVIEW ARTICLE  

Procedural sedation and analgesia in pediatric patients p. 1
Charu Mahajan, Hari Hara Dash
DOI:10.4103/1817-1745.131469  PMID:24891893
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ORIGINAL ARTICLES Top

Umbilical artery pH at birth and neurobehavioral outcome in early preterm infants: A cohort study p. 7
Bhavna Seth, Vikram Datta, Bhanu Kiran Bhakhri
DOI:10.4103/1817-1745.131470  PMID:24891894
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Menkes disease – An important cause of early onset refractory seizures p. 11
Puneet Jain, Lakshminarayanan Kannan, Biswaroop Chakrabarty, Atin Kumar, Neerja Gupta, Madhulika Kabra, Sheffali Gulati
DOI:10.4103/1817-1745.131471  PMID:24891895
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Assessment of parent reported quality of life in children with epilepsy from Northern India: A cross-sectional study p. 17
Vandana Arya, Virender Kumar Gehlawat, Jaya Shankar Kaushik, Geeta Gathwala
DOI:10.4103/1817-1745.131473  PMID:24891896
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CASE REPORTS Top

Infected lumbar dermoid cyst mimicking intramedullary spinal cord tumor: Observations and outcomes p. 21
Sudhakar Vadivelu, Sohum K Desai, Anna Illner, Thomas G Luerssen, Andrew Jea
DOI:10.4103/1817-1745.131475  PMID:24891897
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Aplasia cutis congenita associated with type I split cord malformation: Unusual case p. 27
Bashar Abuzayed, Pamir Erdincler
DOI:10.4103/1817-1745.131477  PMID:24891898
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Thoracic congenital dermal sinus associated with intramedullary spinal dermoid cyst p. 30
Sudhansu Sekhar Mishra, Souvagya Panigrahi
DOI:10.4103/1817-1745.131478  PMID:24891899
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Craniosynostosis in a child with I-cell disease: The need for genetic analysis before contemplating surgery in craniosynostosis p. 33
Lakshmanarao Chittem, Suchanda Bhattacharjee, Prajnya Ranganath
DOI:10.4103/1817-1745.131480  PMID:24891900
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Unusual phenotype of glucose transport protein type 1 deficiency syndrome: A case report and literature review Highly accessed article p. 36
Annio Posar, Margherita Santucci
DOI:10.4103/1817-1745.131481  PMID:24891901
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Paroxysmal vascular events in Sturge– Weber syndrome: Role of aspirin p. 39
Jyoti Sanghvi, Sudhir Mehta, Swati Mulye
DOI:10.4103/1817-1745.131483  PMID:24891902
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Unusual presentation of poststreptococcal glomerulonephritis as posterior reversible encephalopathy syndrome p. 42
Syed Ahmed Zaki, Preeti Shanbag
DOI:10.4103/1817-1745.131484  PMID:24891903
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Cerebral astroblastoma: A radiopathological diagnosis p. 45
Deepak Kumar Singh, Neha Singh, Ragini Singh, Nuzhat Husain
DOI:10.4103/1817-1745.131485  PMID:24891904
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Desmoplastic infantile ganglioglioma: Report of an unusual case with a cranial defect p. 48
Recep Basaran, Fatma Betul Cakir, Nejat Isik, Aydin Sav, Ilhan Elmaci
DOI:10.4103/1817-1745.131486  PMID:24891905
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Intrinsic brainstem white epidermoid cyst: An unusual case report p. 52
Sudhansu Sekhar Mishra, Souvagya Panigrahi, Manmath Kumar Dhir, Acharya Suryakant Pattajoshi
DOI:10.4103/1817-1745.131487  PMID:24891906
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Very severe spinal muscular atrophy: Type 0 with Dandy-Walker variant p. 55
Geeta Gathwala, Joginder Silayach, Bhanu Kiran Bhakhari, Varun Narwal
DOI:10.4103/1817-1745.131488  PMID:24891907
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Catatonia as presenting clinical feature of subacute sclerosing panencephalitis p. 57
Prabhoo Dayal, Yatan Pal Singh Balhara
DOI:10.4103/1817-1745.131489  PMID:24891908
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Auto cannibalism in mental retardation p. 60
Rohit Verma, Shaily Mina, Ankur Sachdeva
DOI:10.4103/1817-1745.131491  PMID:24891909
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A distinct phenotype of childhood leukodystrophy presenting as absence seizure p. 63
Imad Mohammad Dweikat, Nadera Damsah, Reham Khalaf
DOI:10.4103/1817-1745.131492  PMID:24891910
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Garcia-Hafner-Happle syndrome: A case report and review of a rare sub-type of epidermal nevus syndrome Highly accessed article p. 66
Soaham Dilip Desai, Rita Vora, Sheela Bharani
DOI:10.4103/1817-1745.131493  PMID:24891911
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Pontocerebellar hypoplasia type 1 with a milder phenotype in a two-year-old girl p. 70
Puneet Jain, Suvasini Sharma, Atin Kumar, Satinder Aneja
DOI:10.4103/1817-1745.131494  PMID:24891912
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Giant primary cerebral hydatid cyst: A rare cause of childhood seizure p. 73
Shilpa Khanna Arora, Anju Aggarwal, Varsha Datta
DOI:10.4103/1817-1745.131495  PMID:24891913
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Pediatric bilateral large concurrent thalamic glioblastoma: An unusual case report p. 76
Nityanand Pandey, Pankaj Kumar Singh, Ashok K Mahapatra, Aanchal Kakkar, Bhawani Shankar Sharma
DOI:10.4103/1817-1745.131496  PMID:24891914
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A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS p. 79
Giovanna Vitaliti, Rosario R Trifiletti, Raffaele Falsaperla, Enrico Parano, Alberto Spalice, Piero Pavone
DOI:10.4103/1817-1745.131497  PMID:24891915
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Recurrent encephalopathy? No I'm a sleeping beauty! p. 82
Mehtab Iqbal, Manish Prasad, Christopher Ritey
DOI:10.4103/1817-1745.131498  PMID:24891916
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LETTERS TO THE EDITOR Top

Pfeiffer syndrome p. 85
Mitul B Kalathia, Yogesh N Parikh, Meera D Dhami, Palak T Hapani
DOI:10.4103/1817-1745.131499  PMID:24891917
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Baclofen induced coma in an infant p. 86
Syed Ahmed Zaki, Yogesh Gopalrao Khanage
DOI:10.4103/1817-1745.131500  PMID:24891918
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A novel case of 'muscle eye brain disease' in an immigrant family in India p. 88
Vikram S Kumar, VB Sangeeta, KS Shubrata, AV Nagaraja
DOI:10.4103/1817-1745.131501  PMID:24891919
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Traumatic enlargement of an intradiploic cavernous hemangioma p. 90
Amit Mahore, Raghvendra Ramdasi, Anvita Pauranik, Naina Goel
DOI:10.4103/1817-1745.131502  PMID:24891920
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Tectal glioma with hydrocephalus presenting with spastic and ataxic quadriparesis p. 91
Dhaval Shukla, Parayil Sankaran Bindu, Bhagvatula Indira Devi
DOI:10.4103/1817-1745.131505  PMID:24891921
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