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Features
Assistant
AI grounded in research
Search
Full-text citation search
Collections
Organize and monitor papers
All Features →
Integrations
MCP
Connect AI agents to Scite
API
Programmatic data access
Holdings
Full-text via your library
Zotero Plugin
Citation data in Zotero
Browser Extension
Citation badges anywhere
All Integrations →
Data
Rankings
Pricing
Log In
Start Free Trial
Haluk Topaloğlu
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560
Publications
19,654
Citation Statements Received
9,594
Citation Statements Given
How they've been cited
23,420
637
18,947
70
How they cite others
10,800
357
9,192
45
Affiliations
Hacettepe University
,
Hacettepe University Hospital
Publications
Order By: Most citations
Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
Finkel
1
,
Mercuri
2
,
Darras
3
et al.
2017
N Engl J Med
Abstract
Show
2,514
51
2,156
7
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Cite
Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care
Mercuri
1
,
Finkel
2
,
Wirth
3
et al.
2018
Neuromuscular Disorders
Abstract
Show
1,110
12
1,040
1
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Cite
European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision
Van den Bergh
1
,
van Doorn
2
,
Hadden
3
et al.
2021
J Peripheral Nervous Sys
Abstract
Show
540
12
834
3
2
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Add to collection
Cite
The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations
Bladen
1
,
Salgado
2
,
Monges
3
et al.
2015
Human Mutation
Abstract
Show
770
27
762
3
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Cite
European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision
Van den Bergh
1
,
van Doorn
2
,
Hadden
3
et al.
2021
Euro J of Neurology
Abstract
Show
552
22
742
1
2
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Cite
Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: Interim efficacy and safety results from the Phase 2 NURTURE study
De Vivo
1
,
Bertini
2
,
Swoboda
3
et al.
2019
Neuromuscular Disorders
Abstract
Show
669
24
605
1
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Cite
Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1
Yoshida
1
,
Kobayashi
2
,
Manya
3
et al.
2001
Developmental Cell
Abstract
Show
700
6
492
0
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Cite
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan
Godfrey
1
,
Clement
2
,
Mein
3
et al.
2007
Brain
Abstract
Show
443
13
383
0
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Cite
1
2
3
4