- Clinical spectrum in CADASIL family with a new mutation2013 | 1. lékařská fakulta, Ústřední knihovna, 3. lékařská fakulta
- Klinické spektrum antifosfolipidového syndromu1997 | 2. lékařská fakulta
- DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects2015 | 2. lékařská fakulta
- Clinical Spectrum of Mitochondrial Disorders in 76 ChildrenPublikace bez příslušnosti k fakultě
- Laboratory reporting on the clinical spectrum of CFTR p.Arg117His: Still room for improvement2020 | 2. lékařská fakulta
- The Clinical Spectrum of Mitochondrial Disease in 75 Pediatric Patients2003 | 1. lékařská fakulta
- The Clinical Spectrum of Mitochondrial Disease in 75 Pediatric Patients2003 | Fakulta tělesné výchovy a sportu
- Pontocerebellar hypoplasia type 1 Clinical spectrum and relevance of EXOSC3 mutations2013 | 2. lékařská fakulta
- Prevalence Estimates of Amyloid Abnormality Across the Alzheimer Disease Clinical Spectrum2022 | 2. lékařská fakulta
- Extending the clinical spectrum of SPG3A mutations to a very severe and very early complicated phenotype2008 | 2. lékařská fakulta
- Obliterative Lower Airway Lesions in Childhood: Bronchoscopic Diagnosis and Clinical Spectrum2014 | 2. lékařská fakulta
- Outcome measures for children with mitochondrial disease: consensus recommendations for future studies from a Delphi-based international workshop2018 | 1. lékařská fakulta
- Novel SBF2 mutations and clinical spectrum of Charcot-Marie-Tooth neuropathy type 4B22018 | 2. lékařská fakulta
- Clinical spectrum and features of activated phosphoinositide 3-kinase delta syndrome: A large patient cohort study2017 | 2. lékařská fakulta
- Subregional Structural Alterations in Hippocampus and Nucleus Accumbens Correlate with the Clinical Impairment in Patients with Alzheimers Disease Clinical Spectrum: Parallel Combining Volume and Vertex-Based Approach2017 | 2. lékařská fakulta
- Bolesti břicha2012 | 1. lékařská fakulta
- Diferenciální diagnostika selárních expanzí2015 | 1. lékařská fakulta
- Tumors of the hand2017 | 1. lékařská fakulta
- PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature2018 | 2. lékařská fakulta
- Lymeská borelióza2005 | 2. lékařská fakulta
- Periferní neuropatie u Whippleovy choroby: Popis případu2012 | 2. lékařská fakulta
- GRN mutation in a patient with a behavioral variant of frontotemporal lobar degeneration (bvFTD)2017 | Publikace bez příslušnosti k fakultě
- Genetika hereditárních spastických paraplegií2019 | 2. lékařská fakulta
- Additional factors underlying pacing induced cardiomyopathy in patients underwent right ventricular pacing and his bundle pacing. Author's reply2023 | 3. lékařská fakulta
- Globular Glial Tauopathy Type I Presenting as Atypical Progressive Aphasia, With Comorbid Limbic-Predominant Age-Related TDP-43 Encephalopathy2019 | 1. lékařská fakulta, 3. lékařská fakulta
- Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)2012 | 2. lékařská fakulta
- Clinical Characteristics of Patients with Tick-Borne Encephalitis (TBE): A European Multicentre Study from 2010 to 20172021 | Lékařská fakulta v Plzni
- Functional gait disorders: A sign-based approach2020 | 1. lékařská fakulta
- Similar recombination-activating gene (RAG) mutations result in similar immunobiological effects but in different clinical phenotypes2014 | 2. lékařská fakulta
- Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathies2015 | 2. lékařská fakulta