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PubPharm (44)
1
High genetic heterogeneity of leukodystrophies in Iranian children : the first report of Iranian Leukodystrophy Registry
enthalten in:
Neurogenetics
| 2023
von
Ashrafi, M.
|
Kameli, R.
|
Hosseinpour, S.
| +48
ErratumIn: Neurogenetics. 2023 Sep 5;:. - PMID 37668767
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2
Correction to : High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry
enthalten in:
Neurogenetics
| 2023
von
Ashrafi, M.
|
Kameli, R.
|
Hosseinpour, S.
| +48
ErratumFor: Neurogenetics. 2023 Oct;24(4):279-289. - PMID 37597066
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3
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry
enthalten in:
Neurogenetics
| 2023
von
Ashrafi, M.
|
Kameli, R.
|
Hosseinpour, S.
| +48
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4
Correction : Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Dehnavi, A.
|
Bemanalizadeh, M.
|
Kahani, S.
| +14
ErratumFor: Orphanet J Rare Dis. 2023 Jul 5;18(1):177. - PMID 37403138
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5
Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Dehnavi, A.
|
Bemanalizadeh, M.
|
Kahani, S.
| +14
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6
Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Dehnavi, A.
|
Bemanalizadeh, M.
|
Kahani, S.
| +14
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7
Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Dehnavi, A.
|
Bemanalizadeh, M.
|
Kahani, S.
| +14
ErratumIn: Orphanet J Rare Dis. 2023 Jul 17;18(1):190. - PMID 37461050
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8
Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Dehnavi, A.
|
Bemanalizadeh, M.
|
Kahani, S.
| +14
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9
Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Dehnavi, A.
|
Bemanalizadeh, M.
|
Kahani, S.
| +14
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10
Editorial : Assessing and evaluating the impact of the COVID-19 pandemic on anxiety and stress: perspectives from North America
enthalten in:
Frontiers in psychiatry
| 2023
von
Salehi, M.
|
Amanat, M.
|
Garakani, A.
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44
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8
Orphanet journal of rare diseases
4
BMC neurology
3
Cephalalgia : an international journal of headache
3
Current psychology
3
Neurogenetics
3
Reviews in the neurosciences
2
BMC psychiatry
2
Journal of affective disorders
2
Journal of child neurology
2
Journal of interpersonal violence
2
Stem cell research & therapy
1
Drug discovery today
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Expert review of neurotherapeutics
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International journal of injury control and saf...
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Journal of neuroscience research
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Movement disorders : official journal of the Mo...
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Neuropediatrics
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Pharmaceutics
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ResearchSquare.com
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Thema
20
Journal Article
5
Randomized Controlled Trial
5
Research Support, Non-U.S. Gov't
5
Review
5
children
4
Cerebral palsy
4
Children
4
Letter
3
Anxiety
3
Diagnostic Validity
3
INAD
3
Iran
3
MCMI-IV
3
Mutation
3
Neuroaxonal dystrophy
3
PLAN
3
Personality Disorders
3
Psychopathology
3
mortality
2
-associated dystonia–parkinsonism
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Erscheinungszeitraum
33
2020-
11
2010-2019
Erscheinungsjahr(e)
Von:
Bis:
Sprache
44
Englisch
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