[Molecular analysis in hereditary neuromuscular diseases]

[Distribution of the A(TA)7TAA genotype associated with Gilbert syndrome in the Spanish population].

Medicina clinica·2001

[Importance of molecular diagnosis in the detection of healthy male transmitters of the fragile X syndrome].

Anales espanoles de pediatria·1992

[Detection of carriers and diagnosis of Duchenne's muscular dystrophy by DNA analysis].

Anales espanoles de pediatria·1988

[Langerhans' cell histiocytosis: various manifestations with the same histopathologic base].

Anales espanoles de pediatria·2002

[External ventricular assist devices as circulatory support in patients with dilated cardiomyopathy].

Anales espanoles de pediatria·2002

[Comparison of the epidemiological characteristics of neural tube defects classified according to failure of the different points of closure].

Anales espanoles de pediatria·2002

[Cutaneous colonization by Malassezia spp. in neonates].

Anales espanoles de pediatria·2002

[Balloon valvoplasty for critical aortic valve stenosis in neonates].

Anales espanoles de pediatria·2002

[Childhood headache. A diagnostic approach].

Anales espanoles de pediatria·2002

Recurrent giant neurofibroma of the posterior neck and upper back with failed primary grafting and salvage reconstruction: a case report.

Frontiers in surgery·2026

Neuroplasticity After Stroke: Clinical Evidence and Its Implication for Effective Rehabilitation Strategies.

Brain & NeuroRehabilitation·2026

Infection-driven gut dysbiosis and epigenetic programming of microglia: toward a systems level framework linking microbial metabolites, neuroinflammation, synaptic dysfunction, and probiotic modulation.

Frontiers in cellular and infection microbiology·2026

Artificial intelligence-based 3D segmentation of tangle-associated TDP-43 in neurodegeneration.

Brain pathology (Zurich, Switzerland)·2026

Incidence of Tetraplegia After Cervical Laminectomy Versus Laminoplasty: A Propensity Score Matched Analysis Using US Collaborative Network Database in TriNetX.

Global spine journal·2026

Expanded ATXN3 CAG Repeat is Stable in Human Purkinje Cells.

Movement disorders : official journal of the Movement Disorder Society·2026

Related Experiment Videos

[Molecular analysis in hereditary neuromuscular diseases]

Related Concept Videos

[Distribution of the A(TA)7TAA genotype associated with Gilbert syndrome in the Spanish population].

[Importance of molecular diagnosis in the detection of healthy male transmitters of the fragile X syndrome].

[Detection of carriers and diagnosis of Duchenne's muscular dystrophy by DNA analysis].

[Langerhans' cell histiocytosis: various manifestations with the same histopathologic base].

[External ventricular assist devices as circulatory support in patients with dilated cardiomyopathy].

[Comparison of the epidemiological characteristics of neural tube defects classified according to failure of the different points of closure].

[Cutaneous colonization by Malassezia spp. in neonates].

[Balloon valvoplasty for critical aortic valve stenosis in neonates].

[Childhood headache. A diagnostic approach].

Recurrent giant neurofibroma of the posterior neck and upper back with failed primary grafting and salvage reconstruction: a case report.

Neuroplasticity After Stroke: Clinical Evidence and Its Implication for Effective Rehabilitation Strategies.

Infection-driven gut dysbiosis and epigenetic programming of microglia: toward a systems level framework linking microbial metabolites, neuroinflammation, synaptic dysfunction, and probiotic modulation.

Artificial intelligence-based 3D segmentation of tangle-associated TDP-43 in neurodegeneration.

Incidence of Tetraplegia After Cervical Laminectomy Versus Laminoplasty: A Propensity Score Matched Analysis Using US Collaborative Network Database in TriNetX.

Expanded ATXN3 CAG Repeat is Stable in Human Purkinje Cells.

Related Experiment Videos

[Molecular analysis in hereditary neuromuscular diseases]

Related Concept Videos

Related Articles