[Hearing loss in Turner syndrome]

Incidence of myeloproliferative neoplasms - trends by subgroup and age in a population-based study in Sweden.

Journal of internal medicine·2020

Prevalence of myeloma precursor state monoclonal gammopathy of undetermined significance in 12372 individuals 10-49 years old: a population-based study from the National Health and Nutrition Examination Survey.

Blood cancer journal·2017

Synkinesis in Bell's palsy in a randomised controlled trial.

Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery·2016

Peripheral facial palsy: Speech, communication and oral motor function.

European annals of otorhinolaryngology, head and neck diseases·2016

Elevated risk of venous but not arterial thrombosis in Waldenström macroglobulinemia/lymphoplasmacytic lymphoma.

Journal of thrombosis and haemostasis : JTH·2014

Limited evidence for the use of imaging to detect prostate cancer: a systematic review.

European journal of radiology·2014

[Virtually planned correction of a forearm malunion with 3D-technology, a case presentation].

Lakartidningen·2026

[GynOp - the Swedish National Quality Register of Gynecological Surgery].

Lakartidningen·2026

[From somatic symptoms to severe depression - the value of considering atypical presentation and ECT].

Lakartidningen·2026

[Parents advice to staff caring for children with cancer].

Lakartidningen·2026

[Access to health data for research].

Lakartidningen·2026

[CANVAS and RFC1-related disease - a broad clinical spectrum from cough and neuropathy to cerebellar ataxia].

Lakartidningen·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

Related Experiment Videos

[Hearing loss in Turner syndrome]

Related Concept Videos

Incidence of myeloproliferative neoplasms - trends by subgroup and age in a population-based study in Sweden.

Prevalence of myeloma precursor state monoclonal gammopathy of undetermined significance in 12372 individuals 10-49 years old: a population-based study from the National Health and Nutrition Examination Survey.

Synkinesis in Bell's palsy in a randomised controlled trial.

Peripheral facial palsy: Speech, communication and oral motor function.

Elevated risk of venous but not arterial thrombosis in Waldenström macroglobulinemia/lymphoplasmacytic lymphoma.

Limited evidence for the use of imaging to detect prostate cancer: a systematic review.

[Virtually planned correction of a forearm malunion with 3D-technology, a case presentation].

[GynOp - the Swedish National Quality Register of Gynecological Surgery].

[From somatic symptoms to severe depression - the value of considering atypical presentation and ECT].

[Parents advice to staff caring for children with cancer].

[Access to health data for research].

[CANVAS and RFC1-related disease - a broad clinical spectrum from cough and neuropathy to cerebellar ataxia].

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Related Experiment Videos

[Hearing loss in Turner syndrome]

Related Concept Videos

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