[Infantile spinal muscular atrophy. An unusual disease with various differential diagnoses]

Broader phenotypic traits and widespread brain hypometabolism in spinocerebellar ataxia 27.

Journal of internal medicine·2020

Hematopoietic SCT: a useful treatment for late metachromatic leukodystrophy.

Bone marrow transplantation·2014

A novel NGFB point mutation: a phenotype study of heterozygous patients.

Journal of neurology, neurosurgery, and psychiatry·2008

Multiple MAG peptides are recognized by circulating T and B lymphocytes in polyneuropathy and multiple sclerosis.

European journal of neurology·2002

Antiretroviral therapy may improve sensory function in HIV-infected patients: a pilot study.

Neurology·2000

Polyneuropathy in late Lyme borreliosis - a clinical, neurophysiological and morphological description.

Acta neurologica Scandinavica·2000

[Upper tract urothelial carcinoma - regional differences observed in several quality indicators].

Lakartidningen·2026

[Rare manifestations of giant cell arteritis].

Lakartidningen·2026

[Neoehrlichiosis in rituximab-treated patients with MS in Sweden].

Lakartidningen·2026

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

Lakartidningen·2026

[Postoperative atrial fibrillation after open heart surgery].

Lakartidningen·2026

[Interaction between psychotic patients and AI-driven chatbots].

Lakartidningen·2026

Hepatic Steatosis Complicating Pediatric Idiopathic Nephrotic Syndrome During Systemic Corticosteroid Therapy: A Case Report.

Cureus·2026

Umbilical artery bypass for surgical treatment of femoral artery stenosis in a newborn: A case report.

Journal of vascular surgery cases and innovative techniques·2026

Association between 24-hour urine output during early non-invasive ventilation and short-term adverse outcomes in late preterm infants: a retrospective cohort study.

Translational pediatrics·2026

Development and validation of a risk prediction model for respiratory tract Ureaplasma urealyticum infection in preterm infants.

Translational pediatrics·2026

Ultrasound-based nomogram for predicting high-risk hepatic portal venous gas in children: a retrospective cohort study.

Translational pediatrics·2026

Related Experiment Videos

[Infantile spinal muscular atrophy. An unusual disease with various differential diagnoses]

Related Concept Videos

Broader phenotypic traits and widespread brain hypometabolism in spinocerebellar ataxia 27.

Hematopoietic SCT: a useful treatment for late metachromatic leukodystrophy.

A novel NGFB point mutation: a phenotype study of heterozygous patients.

Multiple MAG peptides are recognized by circulating T and B lymphocytes in polyneuropathy and multiple sclerosis.

Antiretroviral therapy may improve sensory function in HIV-infected patients: a pilot study.

Polyneuropathy in late Lyme borreliosis - a clinical, neurophysiological and morphological description.

[Upper tract urothelial carcinoma - regional differences observed in several quality indicators].

[Rare manifestations of giant cell arteritis].

[Neoehrlichiosis in rituximab-treated patients with MS in Sweden].

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

[Postoperative atrial fibrillation after open heart surgery].

[Interaction between psychotic patients and AI-driven chatbots].

Hepatic Steatosis Complicating Pediatric Idiopathic Nephrotic Syndrome During Systemic Corticosteroid Therapy: A Case Report.

Umbilical artery bypass for surgical treatment of femoral artery stenosis in a newborn: A case report.

Association between 24-hour urine output during early non-invasive ventilation and short-term adverse outcomes in late preterm infants: a retrospective cohort study.

Development and validation of a risk prediction model for respiratory tract Ureaplasma urealyticum infection in preterm infants.

Ultrasound-based nomogram for predicting high-risk hepatic portal venous gas in children: a retrospective cohort study.

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[Infantile spinal muscular atrophy. An unusual disease with various differential diagnoses]

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