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  • 1-10 ل  2,536 نتائج ل ""Hereditary""

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Subject : medicine.symptom
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Hereditary hemorrhagic telangiectasia with liver cirrhosis: a case report

Subjects: Male; medicine.medical_specialty; Gastrointestinal bleeding

  • Source: BMC Gastroenterology, Vol 21, Iss 1, Pp 1-6 (2021)BMC Gastroenterology

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The role of C1 inhibitor and complement as acute phase reactants: are we missing the diagnosis of hereditary angioedema?

Subjects: medicine.medical_specialty; Allergy; Complement

  • Source: Allergy, Asthma & Clinical Immunology, Vol 17, Iss 1, Pp 1-4 (2021)Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology

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Early Data on Long-term Impact of Inotersen on Quality-of-Life in Patients with Hereditary Transthyretin Amyloidosis Polyneuropathy: Open-Label Extension of NEURO-TTR

Subjects: Quality of life; medicine.medical_specialty; Neurology

  • Source: Neurology and Therapy

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Pathophysiology and underlying mechanisms in hereditary angioedema

Subjects: Kallikrein-Kinin System; Bradykinin; Inflammation

  • Source: Balkan Medical Journal, Vol 38, Iss 2, Pp 82-88 (2021)

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Genetics & Epigenetics of Hereditary Deafness: An Historical Overview

Subjects: medicine.medical_specialty; epigenetics; Hearing loss

  • Source: Audiology ResearchAudiology Research, Vol 11, Iss 57, Pp 629-635 (2021)

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Recognition and Management of Hereditary Angioedema: Best Practices for Dermatologists

Subjects: Hereditary angioedema; medicine.medical_specialty; C1 inhibitor

  • Source: Dermatology and Therapy

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Microscope Integrated Optical Coherence Tomography Guided Descemet Stripping Automated Endothelial Keratoplasty in Congenital Hereditary Endothelial Dystrophy

Subjects: medicine.medical_specialty; Visual acuity; genetic structures

  • Source: Clinical Ophthalmology (Auckland, N.Z.)

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Initial Cerebellar Ataxia in Hereditary Adult-Onset Primary Lateral Sclerosis

Subjects: Case Series – General Neurology; Pediatrics; medicine.medical_specialty

  • Source: Case Reports in Neurology, Vol 13, Iss 2, Pp 414-421 (2021)Case Reports in Neurology

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A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report

Subjects: Heterozygote; Hereditary spastic paraplegia; [SDV]Life Sciences [q-bio]

  • Source: BMC Neurology, Vol 21, Iss 1, Pp 1-5 (2021)BMC NeurologyBMC Neurology, 2021, 21 (1), pp.78. ⟨10.1186/s12883-021-02113-y⟩BMC Neurology, BioMed Central, 2021, 21 (1), pp.78.

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Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene

Subjects: lcsh:Immunologic diseases. Allergy; medicine.medical_specialty; Pediatrics

  • Source: Clinical and Molecular Allergy, Vol 19, Iss 1, Pp 1-8 (2021)Clinical and Molecular Allergy : CMA

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  • 1-10 ل  2,536 نتائج ل ""Hereditary""