ℹ️
🇬🇧
Search
Search for publications relevant for "clinical spectrum"
clinical spectrum
Publication
Class
Person
Publication
Programmes
publication
Clinical spectrum in CADASIL family with a new mutation
2013 |
First Faculty of Medicine, Central Library of Charles University, Third Faculty of Medicine
publication
Clinical spectrum of the antiphospholipid syndrome
1997 |
Second Faculty of Medicine
publication
DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects
2015 |
Second Faculty of Medicine
publication
Clinical Spectrum of Mitochondrial Disorders in 76 Children
Publication without faculty affiliation
publication
Laboratory reporting on the clinical spectrum of CFTR p.Arg117His: Still room for improvement
2020 |
Second Faculty of Medicine
publication
The Clinical Spectrum of Mitochondrial Disease in 75 Pediatric Patients
2003 |
First Faculty of Medicine
publication
The Clinical Spectrum of Mitochondrial Disease in 75 Pediatric Patients
2003 |
Faculty of Physical Education and Sport
publication
Pontocerebellar hypoplasia type 1 Clinical spectrum and relevance of EXOSC3 mutations
2013 |
Second Faculty of Medicine
publication
Prevalence Estimates of Amyloid Abnormality Across the Alzheimer Disease Clinical Spectrum
2022 |
Second Faculty of Medicine
publication
Extending the clinical spectrum of SPG3A mutations to a very severe and very early complicated phenotype
2008 |
Second Faculty of Medicine
publication
Obliterative Lower Airway Lesions in Childhood: Bronchoscopic Diagnosis and Clinical Spectrum
2014 |
Second Faculty of Medicine
publication
Outcome measures for children with mitochondrial disease: consensus recommendations for future studies from a Delphi-based international workshop
2018 |
First Faculty of Medicine
publication
Novel SBF2 mutations and clinical spectrum of Charcot-Marie-Tooth neuropathy type 4B2
2018 |
Second Faculty of Medicine
publication
Clinical spectrum and features of activated phosphoinositide 3-kinase delta syndrome: A large patient cohort study
2017 |
Second Faculty of Medicine
publication
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 Approach
2017 |
Second Faculty of Medicine
publication
Abdominal pain
2012 |
First Faculty of Medicine
publication
Differential diagnosis of sellar masses
2015 |
First Faculty of Medicine
publication
Tumors of the hand
2017 |
First Faculty of Medicine
publication
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature
2018 |
Second Faculty of Medicine
publication
Lyme borreliosis
2005 |
Second Faculty of Medicine
publication
Peripheral neuropathy in Whipple’s disease: A case report
2012 |
Second Faculty of Medicine
publication
GRN mutation in a patient with a behavioral variant of frontotemporal lobar degeneration (bvFTD)
2017 |
Publication without faculty affiliation
publication
Genetics of hereditary spastic paraplegias
2019 |
Second Faculty of Medicine
publication
Additional factors underlying pacing induced cardiomyopathy in patients underwent right ventricular pacing and his bundle pacing. Author's reply
2023 |
Third Faculty of Medicine
publication
Globular Glial Tauopathy Type I Presenting as Atypical Progressive Aphasia, With Comorbid Limbic-Predominant Age-Related TDP-43 Encephalopathy
2019 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)
2012 |
Second Faculty of Medicine
publication
Clinical Characteristics of Patients with Tick-Borne Encephalitis (TBE): A European Multicentre Study from 2010 to 2017
2021 |
Faculty of Medicine in Pilsen
publication
Functional gait disorders: A sign-based approach
2020 |
First Faculty of Medicine
publication
Similar recombination-activating gene (RAG) mutations result in similar immunobiological effects but in different clinical phenotypes
2014 |
Second Faculty of Medicine
publication
Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathies
2015 |
Second Faculty of Medicine