Suchergebnisse - infantile parkinsonism

1

Diagnosis of autism in a rare case of tyrosine hydroxylase deficiency: a case report

von: Reyes, Zoe Maria Dominique

2023, in: BMC medical genomics

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2

Movement disorders in

von: Di Lazzaro, Giulia

2020, in: Parkinsonism & related disorders

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3

Study of a fetal brain affected by a severe form of tyrosine hydroxylase deficiency, a rare cause of early parkinsonism

von: Tristán-Noguero, Alba

2015, in: Metabolic brain disease

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4

Walking backwards in sports training аnd medical rehabilitation

von: A. Klemenov

2020, in: Спортивная медицина: наука и практика

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5

Consensus guideline for the diagnosis and treatment of aromatic l-amino acid decarboxylase (AADC) deficiency

von: Wassenberg, Tessa

2017, in: Orphanet journal of rare diseases

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6

Co-occurring WARS2 and CHRNA6 mutations in a child with a severe form of infantile parkinsonism

von: Martinelli, Simone

2020, in: Parkinsonism & related disorders

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7

Dopamine Transporter Deficiency Syndrome (DTDS): Expanding the Clinical Phenotype and Precision Medicine Approaches

von: Joanne Ng

2023, in: Cells

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8

Diagnosis of autism in a rare case of tyrosine hydroxylase deficiency: a case report

von: Zoe Maria Dominique Reyes

2023, in: BMC Medical Genomics

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9

Tyrosine hydroxylase deficiency—Clinical insights and a novel deletion in TH gene in an Indian patient

von: Sunita Bijarnia‐Mahay

2020, in: JIMD Reports

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10

PLA2G6-associated neurodegeneration in four different populations-case series and literature review

von: Hanna Al-Shaikh, Rana

2022, in: Parkinsonism & related disorders

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