ISSN: 0387-7604
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Brain and Development Q2 Unclaimed
Brain and Development is a journal indexed in SJR in Medicine (miscellaneous) and Neurology (clinical) with an H index of 96. It has a price of 2650 €. It has an SJR impact factor of 0,498 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,498.
Brain and Development focuses its scope in these topics and keywords: earlyonset, encephalopathy, infantile, epileptic, therapy, disordersradiological, encephalopathies, findings, disordersepilepsy, eeg, ...
Type: Journal
Type of Copyright:
Languages: English
Open Access Policy:
Type of publications:
Publication frecuency: -
2650 €
Inmediate OANPD
Embargoed OA0 €
Non OAMetrics
0,498
SJR Impact factor96
H Index85
Total Docs (Last Year)400
Total Docs (3 years)2110
Total Refs629
Total Cites (3 years)373
Citable Docs (3 years)1.47
Cites/Doc (2 years)24.82
Ref/DocOther journals with similar parameters
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Pharmacological Reports Q2
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Aims and Scope
Best articles by citations
Acute transient pseudoatrophy of the brain accompanying measles infection
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View moreOcular findings in muscle-eye-brain (MEB) disease: a follow-up study
View moreSites and temporal changes of gangliosides GM1/GM2 storage in the Niemann-Pick disease type C mouse brain
View moreIneffectiveness of oral coenzyme Q10 supplementation in 3-methylglutaconic aciduria, type 3
View moreSevere infantile congenital myopathy with nemaline and cytoplasmic bodies: a case report
View moreThree types of multicystic encephalomalacia and the analyses of its risk factors
View moreCoefficient of variation of R-R intervals in severe brain damage
View moreCerebral oxygenation and hemodynamics during hyperventilation and sleep in patients with Rett syndrome
View moreDiagnosis and treatment of 6-pyruvoyl-tetrahydropterin synthase deficiency
View moreHyperkinetic behaviour and superimposed concepts response to De Negri's commentary (Brain Dev 1995:17: 146-7)
View moreWest syndrome: etiological and prognostic aspects
View moreTwo different pathological conditions of photoparoxysmal responses in hereditary dentatorubral-pallidoluysian atrophy
View moreA case of poliomyelitis-like syndrome
View moreA further family with epilepsy, dementia and yellow teeth: the Kohlschutter syndrome
View moreCTG trinucleotide repeat length and clinical expression in a family with myotonic dystrophy
View morePial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy
View moreEffects of blood gas changes on hyperthermia-induced seizures
View moreA case of early-onset benign occipital seizure susceptibility syndrome: decreased cerebral blood flow in the occipital region detected by interictal single photon emission computed tomography, corresponding to the epileptogenic focus
View moreEmpty sella in children as a key for diagnosis
View moreThe controversy regarding diagnostic criteria for early myoclonic encephalopathy
View moreA syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers
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