Magnetic resonance imaging of heterotopic gray matter

Prevention of interstitial fibrosis of renal allograft by angiotensin II blockade.

Transplantation proceedings·2006

Observation of new states decaying into Lambda(c)(+)Kappa(-)pi(+) and Lambda(c)(+)Kappa(0)/(s)pi(-).

Physical review letters·2006

Study of J/psi-->pp[over],LambdaLambda[over] and observation of eta(c)-->LambdaLambda[over] at Belle.

Physical review letters·2006

Observation of a near-threshold D(0)D[over](0)pi(0) enhancement in B-->D(0)D[over](0)pi(0)Kappa decay.

Physical review letters·2006

Measurement of D0-->pilnu(Klnu) form factors and absolute branching fractions.

Physical review letters·2006

Measurement of the quark mixing parameter cos2phi1 using time-dependent Dalitz analysis of B0 -->D[KS(0)pi + pi-]h0.

Physical review letters·2006

Pediatric pseudotumor cerebri syndrome: Clinical characteristics, management and outcomes in a single-center cohort.

Brain & development·2026

Neurocognitive outcomes in pediatric brain arteriovenous malformations: a systematic review.

Brain & development·2026

Cytokine profiles in children with PCR-confirmed HHV-6 infection according to seizure occurrence.

Brain & development·2026

National survey of patients with neuromuscular disease and COVID-19 in Japan.

Brain & development·2026

Comparison of oral prednisolone and ACTH therapies in infantile epileptic spasms syndrome: using BASED and E-Chess scores.

Brain & development·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Medicine·2026

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

Stem cell research·2026

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

CNS neuroscience & therapeutics·2026

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

International journal of molecular sciences·2026

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Genes·2026

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Magnetic resonance imaging of heterotopic gray matter

Related Concept Videos

Prevention of interstitial fibrosis of renal allograft by angiotensin II blockade.

Observation of new states decaying into Lambda(c)(+)Kappa(-)pi(+) and Lambda(c)(+)Kappa(0)/(s)pi(-).

Study of J/psi-->pp[over],LambdaLambda[over] and observation of eta(c)-->LambdaLambda[over] at Belle.

Observation of a near-threshold D(0)D[over](0)pi(0) enhancement in B-->D(0)D[over](0)pi(0)Kappa decay.

Measurement of D0-->pilnu(Klnu) form factors and absolute branching fractions.

Measurement of the quark mixing parameter cos2phi1 using time-dependent Dalitz analysis of B0 -->D[KS(0)pi + pi-]h0.

Pediatric pseudotumor cerebri syndrome: Clinical characteristics, management and outcomes in a single-center cohort.

Neurocognitive outcomes in pediatric brain arteriovenous malformations: a systematic review.

Cytokine profiles in children with PCR-confirmed HHV-6 infection according to seizure occurrence.

National survey of patients with neuromuscular disease and COVID-19 in Japan.

Comparison of oral prednisolone and ACTH therapies in infantile epileptic spasms syndrome: using BASED and E-Chess scores.

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

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Magnetic resonance imaging of heterotopic gray matter

Abstract:

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