Suresh N Magge
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Explore the profile of Suresh N Magge including associated specialties, affiliations and a list of published articles.
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58
Citations
538
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Recent Articles
1.
OBrien P, Teti S, Dewar C, Stabingas K, Rana M, Magge S, et al.
J Neurosurg Pediatr
. 2025 Feb;
:1-6.
PMID: 39983111
Objective: Endoscopic sagittal suturectomy (ESS) is commonly offered for sagittal craniosynostosis in infants, but the optimal timing of surgery remains controversial, with many clinicians only offering ESS surgery before 3...
2.
Bonfield C, Alexander A, Birgfeld C, Couture D, David L, French B, et al.
Neurosurg Focus
. 2025 Jan;
58(1):E3.
PMID: 39742514
Objective: Patients with a history of surgery for single-suture craniosynostosis (SSC) as an infant often wish to participate in sports later in childhood. However, there are no established guidelines from...
3.
Motahari Z, Lepe J, Bautista M, Hoerig C, Plant-Fox A, Das B, et al.
PLoS One
. 2024 Oct;
19(10):e0300411.
PMID: 39436961
Methods: DAOY (SHH driven/tp53 mutant) and D425 (non-SHH group 3) were treated with BT9. For in vitro analysis, cell proliferation, death, migration, invasion, and metabolic activity were assessed using MTT...
4.
Robert A, Hanel R, Adelson P, Lang S, Grabb P, Greene S, et al.
J Neurosurg Pediatr
. 2024 Jul;
34(4):402-413.
PMID: 39029127
Objective: Cerebral revascularization surgery (CRS) has been used to prevent stroke in children with sickle cell disease (SCD) and cerebral vasculopathy (e.g., moyamoya syndrome). While results suggest that it may...
5.
Boulter J, Szuflita N, Keating R, Magge S
Childs Nerv Syst
. 2024 May;
40(8):2449-2456.
PMID: 38753003
Purpose: Moyamoya disease and syndrome represent rare entities characterized by progressive stenosis and/or occlusion of the intracranial blood vessels. We present our series of patients with moyamoya disease and syndrome...
6.
Chiang S, Reckford J, Alexander A, Birgfeld C, Bonfield C, Couture D, et al.
J Neurosurg Pediatr
. 2024 May;
34(2):182-189.
PMID: 38728754
Objective: As many as 5% of normocephalic children may have a prematurely fused sagittal suture, yet the clinical significance and best course of management of this finding remain unclear. Providers...
7.
Magge S, Fotouhi A, Allhusen V, Collett B, Skolnick G, Naidoo S, et al.
JAMA Netw Open
. 2024 Apr;
7(4):e248762.
PMID: 38683606
Importance: Several studies have reported a higher incidence of neurodevelopmental delays and cognitive deficits in patients with single-suture craniosynostosis; however, there are few studies examining the associations of repair type...
8.
Motahari Z, Lepe J, Bautista M, Hoerig C, Plant-Fox A, Das B, et al.
bioRxiv
. 2024 Mar;
PMID: 38464047
Methods: Multiple in vitro assays were performed using human DAOY (SHH activated tp53 mutant) and D425 (non-SHH group 3) cells. The impact of BT9 on cellular growth, death, migration, invasion,...
9.
Ahmed S, Allhusen V, Muhonen M, Magge S
Childs Nerv Syst
. 2024 Feb;
40(6):1833-1838.
PMID: 38411706
Purpose: Depressed ("ping-pong") skull fractures can be treated by different means, including observation, non-surgical treatments, or surgical intervention. The authors describe their experience with vacuum-assisted elevation of ping-pong skull fractures...
10.
Mortazavi A, Almeida N, Hofmann K, Davidson L, Rotter J, Phan T, et al.
J Neurosurg Pediatr
. 2024 Feb;
34(1):49-56.
PMID: 38394661
Objective: Treatment for Chiari malformation type I (CM-I) often includes surgical intervention in both pediatric and adult patients. The authors sought to investigate fundamental differences between these populations by analyzing...