Follow-up of 25 patients with treatable ataxia: A comprehensive case series study.
Mahmoud Reza Ashrafi, Elham Pourbakhtyaran, Mohammad Rohani, Bita Shalbafan, Ali Reza Tavasoli, Sareh Hosseinpour, Maryam Rasulinezhad, Zahra Rezaei, Ali Zare Dehnavi, Seyyed Mohammad Mahdi Hosseiny and 3 more
Article in Clinical case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 43% of its field
1 · What the graph read from it
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
2 · The registry
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
3 · Its place in the literature
Who cites it
3 citing papers in PubMed, 3 citations in OpenAlex.
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what money
Authors and funding
13 authors at 4 institutions in 1 country.
Mahmoud Reza AshrafiDepartment of Paediatrics Division of Paediatric Neurology, Growth and Development Research Center Children's Medical Centre Paediatrics Centre of Excellence Tehran University of Medical Sciences Tehran Iran.
Elham PourbakhtyaranDepartment of Paediatrics Division of Paediatric Neurology, Growth and Development Research Center Children's Medical Centre Paediatrics Centre of Excellence Tehran University of Medical Sciences Tehran Iran.
Mohammad RohaniDepartment of Neurology School of Medicine Hazrat Rasool-E Akram General Hospital Iran University of Medical Sciences Tehran Iran.
Bita ShalbafanClinical Research Development Center of Labbafinejad Hospital Shahid Beheshti University of Medical Sciences Tehran Iran.
Ali Reza TavasoliPediatric Neurology Division Children's Medical Center Pediatrics Center of Excellence Myelin Disorders Clinic Tehran University of Medical Sciences Tehran Iran.
Sareh HosseinpourDepartment of Pediatric Neurology Vali-e-Asr Hospital Imam Khomeini Hospital Complex Tehran University of Medical Sciences Tehran Iran.
Maryam RasulinezhadPediatric Neurology Division Children's Medical Center Pediatrics Center of Excellence Myelin Disorders Clinic Tehran University of Medical Sciences Tehran Iran.
Zahra RezaeiDepartment of Paediatrics Division of Paediatric Neurology, Growth and Development Research Center Children's Medical Centre Paediatrics Centre of Excellence Tehran University of Medical Sciences Tehran Iran.
Ali Zare DehnaviDepartment of Paediatrics Division of Paediatric Neurology, Growth and Development Research Center Children's Medical Centre Paediatrics Centre of Excellence Tehran University of Medical Sciences Tehran Iran.ORCID https://orcid.org/0000-0002-8584-6579
Seyyed Mohammad Mahdi HosseinyPediatric Neurology Division Children's Medical Center Pediatrics Center of Excellence Myelin Disorders Clinic Tehran University of Medical Sciences Tehran Iran.
Roya HaghighiPediatric Neurology Division Children's Medical Center Pediatrics Center of Excellence Myelin Disorders Clinic Tehran University of Medical Sciences Tehran Iran.
Homa GhabeliPediatric Neurology Division Children's Medical Center Pediatrics Center of Excellence Myelin Disorders Clinic Tehran University of Medical Sciences Tehran Iran.
Morteza HeidariDepartment of Paediatrics Division of Paediatric Neurology, Growth and Development Research Center Children's Medical Centre Paediatrics Centre of Excellence Tehran University of Medical Sciences Tehran Iran.ORCID https://orcid.org/0000-0002-7487-569X
Children's Medical Center · IRHospital Labbafinejad · IRImam Khomeini Hospital · IRIran University of Medical Sciences · IR
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itself
Abstract
Autosomal recessive cerebellar ataxias are a group of heterogeneous early-onset progressive disorders that some of them are treatable. We performed a 4-year follow-up for 25 patients who had treatable ataxia. According to our study, patients would benefit from early detection of treatable ataxia, close observation, and follow-up.
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.
Follow-up of 25 patients with treatable ataxia: A comprehensive case series study. · full record | OpenQuestion