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PubPharm (75)
1
Sexual Dimorphism in Telomere Length in Childhood Autism
enthalten in:
bioRxiv.org
| 2024
von
Panahi, Y.
|
Moghaddam, F.
|
Babaei, K.
| +6
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2
Pseudodendritic keratitis in citrullinemia; a report of an unusual and novel ocular finding in this metabolic disorder
enthalten in:
American journal of ophthalmology case reports
| 2024
von
Amirkashani, D.
|
Talebi, S.
|
Vafaei Shahi, M.
| +3
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3
The effects of coenzyme Q10 supplementation on biomarkers of exercise-induced muscle damage, physical performance, and oxidative stress : A GRADE-assessed systematic review and dose-response meta-analysis of randomized controlled trials
enthalten in:
Clinical nutrition ESPEN
| 2024
von
Talebi, S.
|
Pourgharib Shahi, M.
|
Zeraattalab-Motlagh, S.
| +6
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4
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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5
Genetic insights into PHARC syndrome : identification of a novel frameshift mutation in ABHD12
enthalten in:
BMC medical genomics
| 2023
von
Daneshi, A.
|
Garshasbi, M.
|
Farhadi, M.
| +6
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6
Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12
enthalten in:
BMC medical genomics
| 2023
von
Daneshi, A.
|
Garshasbi, M.
|
Farhadi, M.
| +6
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7
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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8
The Effect of Birth Hour on Neonatal Morbidity and Mortality in Very-Low Birth Weight Infants in a Teaching Hospital
enthalten in:
Turkish archives of pediatrics
| 2023
von
Houjaghani, H.
|
Mohammadi, N.
|
Vahedi, Z.
| +2
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9
Influence of Food Type on Human Psychological-Behavioral Responses and Crime Reduction
enthalten in:
Nutrients
| 2023
von
Heidari, M.
|
Khodadadi Jokar, Y.
|
Madani, S.
| +3
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10
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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Medienart
75
Aufsätze
69
E-Artikel
69
E-Ressourcen
6
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Zeitschriftentitel
9
ResearchSquare.com
4
Iranian journal of child neurology
4
Irish journal of medical science
3
BMC dermatology
3
European spine journal
3
Neurogenetics
3
Trials
2
Asian journal of sports medicine
2
BMC medical genomics
2
Foot & ankle specialist
2
Journal of diabetes & metabolic disorders
1
Advances in medicine
1
American journal of ophthalmology case reports
1
Anatolian journal of cardiology
1
BJSM
1
BioMedicine
1
Clinical Case Reports
1
Clinical case reports
1
Clinical neurology and neurosurgery
1
Clinical nutrition ESPEN
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Thema
38
Journal Article
8
Case Reports
8
Whole-exome sequencing
6
Ataxia
4
Aminoacyl-tRNA synthetases
4
Brachymetatarsia
4
COXPD24
4
Competitive sports
4
Lumbar pain
4
NARS2
4
Prevalence
4
Research Support, Non-U.S. Gov't
3
ADHD
3
Attention-deficit/hyperactivity disorder
3
Citrate synthase
3
Complementary and alternative medicines
3
Cytochrome c oxidase
3
Herbal medicine
3
Mitochondrial dysfunction
3
PGC1α
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Erscheinungszeitraum
56
2020-
16
2010-2019
3
2000-2009
Erscheinungsjahr(e)
Von:
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Sprache
74
Englisch
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