[Many bone alterations in Larsen's syndrome]

Significance of tuber size for complications of tuberous sclerosis complex.

Neurologia (Barcelona, Spain)·2013

[Congenital cytomegalovirus infection and cortical/subcortical malformations].

Neurologia (Barcelona, Spain)·2012

Focal cortical dysplasia. Clinical-radiological-pathological associations.

Neurologia (Barcelona, Spain)·2012

Schizencephaly: a study of 16 patients.

Neurologia (Barcelona, Spain)·2011

Cutaneous, mediastinal and hepatic hemangiomas in a girl followed during 12 years.

Neuropediatrics·2011

Persistence of the stapedial artery associated with facial hemangioma: a case report.

Neuropediatrics·2010

<sup>18</sup>F-FDG PET/MRI Multiparametric Imaging Features for Predicting MYCN Amplification Status in Children With High-Risk Neuroblastoma.

Revista de neurologia·2026

Anti-Melanoma Differentiation-Associated Gene 5 Antibody-Positive Juvenile Dermatomyositis Presenting With Predominant Joint Contractures.

Revista de neurologia·2026

Association Between Immunotherapy and Generalization in Ocular Myasthenia Gravis as a Function of Antibody Status.

Revista de neurologia·2026

Systematic Review and Meta-Analysis of the Efficacy of Fecal Microbiota Transplantation in Parkinson's Disease: An Exploration Based on UPDRS and Cognitive Scores.

Revista de neurologia·2026

The Dual Role of VEGF in Intracerebral Haemorrhage: From Pathological Mechanisms to Therapeutic Opportunities.

Revista de neurologia·2026

Statistical Inference in Database Exploitation: Sample Size and Confounding Factors.

Revista de neurologia·2026

Luminescence lifetime imaging integrated into selective plane illumination microscopy for oxygen imaging in 3D cell cultures.

Biomedical optics express·2026

Double-pulse laser capture microdissection with a needle beam for reduced collateral damage in biological samples.

Biomedical optics express·2026

Super-resolving frequency measurement with mode-selective quantum memory.

Nature sensors·2026

Quantifying optical scattering losses in pump-probe serial femtosecond crystallography experiments.

IUCrJ·2026

The infero-apical left ventricular aneurysm and long QT syndrome caused by mutation delKKP 1504-1506 in SCN5A gene.

BMC medical genomics·2026

Channel-resolved excitation trends in Si, GaAs, and NiO for sub-GeV dark matter detection.

Scientific reports·2026

Related Experiment Videos

[Many bone alterations in Larsen's syndrome]

Related Concept Videos

Significance of tuber size for complications of tuberous sclerosis complex.

[Congenital cytomegalovirus infection and cortical/subcortical malformations].

Focal cortical dysplasia. Clinical-radiological-pathological associations.

Schizencephaly: a study of 16 patients.

Cutaneous, mediastinal and hepatic hemangiomas in a girl followed during 12 years.

Persistence of the stapedial artery associated with facial hemangioma: a case report.

<sup>18</sup>F-FDG PET/MRI Multiparametric Imaging Features for Predicting MYCN Amplification Status in Children With High-Risk Neuroblastoma.

Anti-Melanoma Differentiation-Associated Gene 5 Antibody-Positive Juvenile Dermatomyositis Presenting With Predominant Joint Contractures.

Association Between Immunotherapy and Generalization in Ocular Myasthenia Gravis as a Function of Antibody Status.

Systematic Review and Meta-Analysis of the Efficacy of Fecal Microbiota Transplantation in Parkinson's Disease: An Exploration Based on UPDRS and Cognitive Scores.

The Dual Role of VEGF in Intracerebral Haemorrhage: From Pathological Mechanisms to Therapeutic Opportunities.

Statistical Inference in Database Exploitation: Sample Size and Confounding Factors.

Luminescence lifetime imaging integrated into selective plane illumination microscopy for oxygen imaging in 3D cell cultures.

Double-pulse laser capture microdissection with a needle beam for reduced collateral damage in biological samples.

Super-resolving frequency measurement with mode-selective quantum memory.

Quantifying optical scattering losses in pump-probe serial femtosecond crystallography experiments.

The infero-apical left ventricular aneurysm and long QT syndrome caused by mutation delKKP 1504-1506 in SCN5A gene.

Channel-resolved excitation trends in Si, GaAs, and NiO for sub-GeV dark matter detection.

Related Experiment Videos

[Many bone alterations in Larsen's syndrome]

Related Concept Videos

Related Articles