Tag: Autosomal dominant disorders

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Recent Related Articles to Autosomal dominant disorders

'New' Biohaven up 81% days after Pfizer acquisition as investors see pipeline potential

Added to Collection on: 2022-10-06 17:42:45

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Neurological disorders
Health
Organ systems
Rare diseases
Autosomal dominant disorders
Pfizer
Spinocerebellar ataxia
Ataxia
Biohaven Ltd.
Biohaven Pharmaceuticals

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Acute Intermittent Porphyria Market is expected to Grow during Forecast Period (2023-2032 ...

Added to Collection on: 2023-09-14 12:52:52

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Porphyrias
Metabolism
Biomolecules
Autosomal dominant disorders
Porphyrins
Acute intermittent porphyria
Porphobilinogen deaminase
Abdominal pain
Porphobilinogen
AIP
Heme
Givosiran

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Vico Therapeutics Raises $60M in Series B Financing - FinSMEs

Added to Collection on: 2024-01-06 01:57:26

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Rare diseases
Autosomal dominant disorders
Spinocerebellar ataxia
Huntington's disease
Cerebellar ataxia
Ataxia
Trinucleotide repeat disorder
Vico Therapeutics Vico Therapeutics

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Dutch-based Vico Therapeutics secures €54M to develop therapies for neurological diseases

Added to Collection on: 2024-01-05 22:40:01

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Rare diseases
Autosomal dominant disorders
Neurodegenerative disorders
Spinocerebellar ataxia
Machado–Joseph disease
Ataxia
Vico Therapeutics

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Vico Therapeutics Announces $60 million (€54 million) Series B Financing to Advance ... - BioSpace

Added to Collection on: 2024-01-05 20:43:43

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Rare diseases
Autosomal dominant disorders
Trinucleotide repeat disorders
Neurodegenerative disorders
Huntington's disease
Spinocerebellar ataxia
Neurodegenerative disease
Machado–Joseph disease
Ataxia
Cerebellar ataxia
Vico Therapeutics B.V.

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Vico Therapeutics Announces $60 million (€54 million) Series B Financing to Advance ...

Added to Collection on: 2024-01-05 13:27:33

Tags for this article:

Rare diseases
Autosomal dominant disorders
Trinucleotide repeat disorders
Neurodegenerative disorders
Huntington's disease
Spinocerebellar ataxia
Neurodegenerative disease
Machado–Joseph disease
Ataxia
Cerebellar ataxia
Vico Therapeutics B.V.

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Discovery unravels the mystery of a rare bone disease - EurekAlert!

Added to Collection on: 2024-01-20 20:19:32

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Rare diseases
Collagen disease
Congenital disorders
Autosomal dominant disorders
Keutel syndrome
Skeletal disorders
Matrix gla protein
Spondyloepiphyseal dysplasia congenita
Osteochondrodysplasia

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Diagnostic uplift through the implementation of short tandem repeat analysis using exome ...

Added to Collection on: 2024-02-02 17:52:00

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Autosomal dominant disorders
Trinucleotide repeat disorders
Rare diseases
Neurodegenerative disorders
Dentatorubral–pallidoluysian atrophy
Ataxin 7
Spinocerebellar ataxia
Myotonic dystrophy
Exome sequencing
Cerebellar ataxia
Anticipation

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18-Years of single-centre DNA testing in over 7000 index cases with inherited retinal ...

Added to Collection on: 2024-10-26 17:17:13

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Rare diseases
Blindness
Channelopathies
Retinitis pigmentosa
Leber congenital amaurosis
Usher syndrome
Autosomal dominant disorders

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Baby to fly to Mexico for 'life-changing' therapy - BBC

Added to Collection on: 2025-01-02 14:19:00

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Autosomal dominant disorders
Muscular dystrophy
Dystrophy
Myotonic dystrophy
Myotonia
Stem-cell therapy
Celine

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