The mystery of the Rett syndrome

Down syndrome: MR quantification of brain structures and comparison with normal control subjects.

AJNR. American journal of neuroradiology·1991

Peripheral nerve involvement in the Rett syndrome.

Brain & development·1990

A review of the Rett syndrome with a theory of autism.

Brain & development·1990

Glycosphingolipids in patients with the Rett syndrome.

Brain & development·1990

[Assessing refraction in children with cerebral damage].

Klinische Monatsblatter fur Augenheilkunde·1987

Autism and Rett syndrome: behavioural investigations and differential diagnosis.

Developmental medicine and child neurology·1987

Cumulative red flag count as a predictor of intracranial pathology in pediatric emergency headache: A threshold-based analysis.

Brain & development·2026

The relationship between stereotypical movement disorder and neuroinflammation.

Brain & development·2026

Vigabatrin therapy for infantile epileptic spasms syndrome with periventricular leukomalacia.

Brain & development·2026

Natural history of a cohort of children with type 2 spinal muscular atrophy from southern India - A retrospective single-centre study.

Brain & development·2026

Associations of muscle thickness and echo intensity with pneumonia onset in patients with severe cerebral palsy: a longitudinal study.

Brain & development·2026

Associations between patterns of diffusion-weighted magnetic resonance imaging and long-term outcomes in acute encephalopathy with biphasic seizures and late reduced diffusion.

Brain & development·2026

Identification of the Novel HLA-A*68:346 Allele in a Brazilian Individual by Next-Generation Sequencing.

HLA·2026

Immunoglobulin Superfamily Protein BTNL9 Functions as a Non-Canonical Transcriptional Regulator to Suppress NSCLC Through Cell Cycle and p53 Pathways.

International journal of molecular sciences·2026

Identification of the Novel HLA-DRB1*04:01:26 Allele by Next-Generation Sequencing.

HLA·2026

The HLA-C*08:01:45 Allele, Identified by Next-Generation Sequencing in an Indian Individual.

HLA·2026

Identification of the Novel HLA-DRB1*11:01:49 Allele Using Next-Generation Sequencing in a Chinese Individual.

HLA·2026

Resolving diagnostic complexity: long-read sequencing unmasks a Hong Kongαα/‒α4.2 genotype mimicking a heterozygous ‒α3.7 deletion on multiplex ligation-dependent probe amplification.

Laboratory medicine·2026

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The mystery of the Rett syndrome

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Down syndrome: MR quantification of brain structures and comparison with normal control subjects.

Peripheral nerve involvement in the Rett syndrome.

A review of the Rett syndrome with a theory of autism.

Glycosphingolipids in patients with the Rett syndrome.

[Assessing refraction in children with cerebral damage].

Autism and Rett syndrome: behavioural investigations and differential diagnosis.

Cumulative red flag count as a predictor of intracranial pathology in pediatric emergency headache: A threshold-based analysis.

The relationship between stereotypical movement disorder and neuroinflammation.

Vigabatrin therapy for infantile epileptic spasms syndrome with periventricular leukomalacia.

Natural history of a cohort of children with type 2 spinal muscular atrophy from southern India - A retrospective single-centre study.

Associations of muscle thickness and echo intensity with pneumonia onset in patients with severe cerebral palsy: a longitudinal study.

Associations between patterns of diffusion-weighted magnetic resonance imaging and long-term outcomes in acute encephalopathy with biphasic seizures and late reduced diffusion.

Identification of the Novel HLA-A*68:346 Allele in a Brazilian Individual by Next-Generation Sequencing.

Immunoglobulin Superfamily Protein BTNL9 Functions as a Non-Canonical Transcriptional Regulator to Suppress NSCLC Through Cell Cycle and p53 Pathways.

Identification of the Novel HLA-DRB1*04:01:26 Allele by Next-Generation Sequencing.

The HLA-C*08:01:45 Allele, Identified by Next-Generation Sequencing in an Indian Individual.

Identification of the Novel HLA-DRB1*11:01:49 Allele Using Next-Generation Sequencing in a Chinese Individual.

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The mystery of the Rett syndrome

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