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A 13-Year-Old Boy with Ataxia 4 Weeks after a Near-Drowning Accident

Clinical infectious diseases, 2010-08, Vol.51 (3), p.326-327

Mackowiak, Philip A

2010

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133Xe inhalation cerebrography (author's transl)

Nō shinkei geka, 1979-03, Vol.7 (3), p.219

1979

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15-White Dots APP-Coo-Test: a reliable touch-screen application for assessing upper limb movement impairment in patients with cerebellar ataxias

Journal of neurology, 2019-07, Vol.266 (7), p.1611-1622

2019

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A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano

Journal of human genetics, 2006-05, Vol.51 (5), p.461-466

2006

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16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study

Journal of the neurological sciences, 2006-09, Vol.247 (2), p.180-186

2006

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16q-linked autosomal dominant cerebellar ataxia in a Korean family

European journal of neurology, 2007-06, Vol.14 (6), p.e16-e17

2007

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16q‐linked autosomal dominant cerebellar ataxia in a Korean family

European journal of neurology, 2007-06, Vol.14 (6), p.e16-e17

2007

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18F-FDG PET in neurodegenerative Langerhans cell histiocytosis: Results and potential interest for an early diagnosis of the disease

Journal of neurology, 2008-04, Vol.255 (4), p.575-580

2008

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18F‐Florzolotau Tau Positron Emission Tomography Imaging in Patients with Multiple System Atrophy–Parkinsonian Subtype

Movement disorders, 2022-09, Vol.37 (9), p.1915-1923

2022

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A 19-year-old male with cerebellar ataxia and cognitive impairment following glandular fever

Journal of clinical neuroscience, 2013-05, Vol.20 (5), p.749-750

2013

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1H MRS spectroscopy evidence of cerebellar high lactate in mitochondrial respiratory chain deficiency

Molecular genetics and metabolism, 2008, Vol.93 (1), p.85-88

2008

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2-[18F]fluoro-2-deoxy-D-glucose PET-CT in a case of cerebellar ataxia associated thyroid disorder

Majallahī-i pizishk-i hastahī Īrān, 2022-07, Vol.30 (2), p.129

2022

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2 aspects of progressive ophthalmoplegia in a heredoataxic sibling group

Acta neurologica et psychiatrica Belgica, 1969-09, Vol.69 (9), p.718

1969

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2 autopsy cases of the spinocerebellar degeneration with cerebral atrophy

No To Shinkei, 1970-10, Vol.22 (10), p.1201

1970

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2 cases of herediary ataxia among brothers

Saishin igaku, 1971-10, Vol.26 (10), p.2002

1971

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2 cases of neuroblastoma with acute cerebellar ataxia

Nihon rinshō, 1975-06, Vol.33 (6), p.2202

1975

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2 cases of spinocerebellar heredoataxia

No To Shinkei, 1962-03, Vol.14, p.205

1962

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2-Halopropionic Acid-induced Cerebellar Granule Cell Necrosis in the Rat: In Vivo and In Vitro Studies

Neurotoxicology (Park Forest South), 2001-06, Vol.22 (3), p.363-374

2001

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L-2-hydroxyglutaric aciduria

Ryoikibetsu shokogun shirizu, 1998 (18 Pt 1), p.392

Terada, N

1998

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L-2-hydroxyglutaric aciduria and brain malignant tumors: a predisposing condition?

Neurology, 2004-05, Vol.62 (10), p.1882

2004

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L-2-hydroxyglutaric aciduria diagnosed in a young adult with progressive cerebellar ataxia and facial dyskinesia

Revue neurologique, 2012-02, Vol.168 (2), p.187-191

2012

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L-2 hydroxyglutaric aciduria: report of a Mexican-Mayan patient with the mutation c.569C>T and response to vitamin supplements and levocarnitine

Tremor and other hyperkinetic movements (New York, N.Y.), 2024, Vol.14 (1), p.12

2024

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A 27-year-old man with ataxia and a left cerebellar mass 13 years after resection and radiation therapy of a left parietal astrocytoma. (includes discussion by case physicians) (Case Records of the Massachusetts General Hospital: Case 23-1991)

The New England journal of medicine, 1991-06, Vol.324 (23), p.1651

1991

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A 29-year-old man with diabetes insipidus and cerebellar ataxia and development of spinal cord swelling 15 years after the onset

No To Shinkei, 1999-02, Vol.51 (2), p.180

Sugiyama, K

1999

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A 29-year-old man with diabetes insipidus and cerebellar ataxia and development of spinal cord swelling 15 years after the onset

No To Shinkei, 1997-05, Vol.49 (5), p.473

1997

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A 13-Year-Old Boy with Ataxia 4 Weeks after a Near-Drowning Accident

133Xe inhalation cerebrography (author's transl)

15-White Dots APP-Coo-Test: a reliable touch-screen application for assessing upper limb movement impairment in patients with cerebellar ataxias

A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano

16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study

16q-linked autosomal dominant cerebellar ataxia in a Korean family

16q‐linked autosomal dominant cerebellar ataxia in a Korean family

18F-FDG PET in neurodegenerative Langerhans cell histiocytosis: Results and potential interest for an early diagnosis of the disease

18F‐Florzolotau Tau Positron Emission Tomography Imaging in Patients with Multiple System Atrophy–Parkinsonian Subtype

A 19-year-old male with cerebellar ataxia and cognitive impairment following glandular fever

1H MRS spectroscopy evidence of cerebellar high lactate in mitochondrial respiratory chain deficiency

2-[18F]fluoro-2-deoxy-D-glucose PET-CT in a case of cerebellar ataxia associated thyroid disorder

2 aspects of progressive ophthalmoplegia in a heredoataxic sibling group

2 autopsy cases of the spinocerebellar degeneration with cerebral atrophy

2 cases of herediary ataxia among brothers

2 cases of neuroblastoma with acute cerebellar ataxia

2 cases of spinocerebellar heredoataxia

2-Halopropionic Acid-induced Cerebellar Granule Cell Necrosis in the Rat: In Vivo and In Vitro Studies

L-2-hydroxyglutaric aciduria

L-2-hydroxyglutaric aciduria and brain malignant tumors: a predisposing condition?

L-2-hydroxyglutaric aciduria diagnosed in a young adult with progressive cerebellar ataxia and facial dyskinesia

L-2 hydroxyglutaric aciduria: report of a Mexican-Mayan patient with the mutation c.569C>T and response to vitamin supplements and levocarnitine

A 27-year-old man with ataxia and a left cerebellar mass 13 years after resection and radiation therapy of a left parietal astrocytoma. (includes discussion by case physicians) (Case Records of the Massachusetts General Hospital: Case 23-1991)

A 29-year-old man with diabetes insipidus and cerebellar ataxia and development of spinal cord swelling 15 years after the onset

A 29-year-old man with diabetes insipidus and cerebellar ataxia and development of spinal cord swelling 15 years after the onset

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