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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 1
1966 2
1967 2
1968 5
1969 6
1970 4
1971 1
1972 4
1973 2
1975 1
1980 1
1981 3
1982 2
1984 2
1985 1
1986 3
1987 4
1988 2
1989 4
1992 1
1993 1
1994 2
1995 4
1996 1
1997 3
1998 3
2000 3
2001 1
2002 2
2003 1
2005 2
2006 3
2007 2
2008 3
2009 4
2010 5
2011 4
2012 2
2013 3
2015 6
2016 2
2018 4
2019 5
2020 3
2024 1

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113 results

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Quoted phrase not found in phrase index: "Progressive sclerosing poliodystrophy"
Page 1
Recurrent schilder's disease.
Dunn-Pirio AM, Eckstein C. Dunn-Pirio AM, et al. Mult Scler Relat Disord. 2018 Nov;26:8-10. doi: 10.1016/j.msard.2018.09.001. Epub 2018 Sep 5. Mult Scler Relat Disord. 2018. PMID: 30212769
Schilder's disease is a rare and aggressive central nervous system demyelinating disorder that is typically monophasic and steroid responsive. Here, we present an unusual case of a teenager with Schilder's disease who was treated with corticosteroids and had a cl …
Schilder's disease is a rare and aggressive central nervous system demyelinating disorder that is typically monophasic and steroid re …
Tumefactive Demyelination Lesions: Report on three cases.
Lin CJ, Lin SC, Yu KW, Ou Yang WY, Lee YC, Liao YC. Lin CJ, et al. Acta Neurol Taiwan. 2024 Dec 30;33(4):195-200. Acta Neurol Taiwan. 2024. PMID: 38073158
This study aims at pinpointing the key neuroimaging features to distinguish TD lesions from surgical conditions, and illustrating the clinical outcomes of patients with TD lesions. CASE REPORT: Two of the three patients had solitary TD lesions, one 47-year-old man presenti …
This study aims at pinpointing the key neuroimaging features to distinguish TD lesions from surgical conditions, and illustrating the cli …
Juvenile Alpers disease.
Wiltshire E, Davidzon G, DiMauro S, Akman HO, Sadleir L, Haas L, Zuccollo J, McEwen A, Thorburn DR. Wiltshire E, et al. Arch Neurol. 2008 Jan;65(1):121-4. doi: 10.1001/archneurol.2007.14. Arch Neurol. 2008. PMID: 18195149
OBJECTIVE: To report a juvenile case of Alpers disease due to mutations in the polymerase gamma gene (POLG1). DESIGN: Clinical, pathologic, biochemical, and molecular analysis. SETTING: Tertiary care university hospital and academic institutions. PATIENT: A 17-year-old ado …
OBJECTIVE: To report a juvenile case of Alpers disease due to mutations in the polymerase gamma gene (POLG1). DESIGN: Clinical, patho …
Mesial temporal sclerosis: pathogenesis and significance.
Liu Z, Mikati M, Holmes GL. Liu Z, et al. Pediatr Neurol. 1995 Jan;12(1):5-16. doi: 10.1016/0887-8994(94)00122-i. Pediatr Neurol. 1995. PMID: 7748361 Review.
Mesial temporal sclerosis (MTS) is a common pathologic finding in patients with temporal lobe epilepsy. ...Although the etiology of MTS remains controversial, there is now a considerable amount of evidence demonstrating that MTS is both a result and a cause of seizures. …
Mesial temporal sclerosis (MTS) is a common pathologic finding in patients with temporal lobe epilepsy. ...Although the etiology of M …
Adrenoleukodystrophy.
Ladenson PW. Ladenson PW. JAMA. 1989 Sep 15;262(11):1504-6. JAMA. 1989. PMID: 2769901 No abstract available.
Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia.
Shapira Y, Cederbaum SD, Cancilla PA, Nielsen D, Lippe BM. Shapira Y, et al. Neurology. 1975 Jul;25(7):614-21. doi: 10.1212/wnl.25.7.614. Neurology. 1975. PMID: 1171391
In two siblings with limb-girdle muscle weakness and episodic headaches and vomiting from early childhood, progressive neurologic degeneration later developed, and both children died. In one child, corticosteroids induced improvement in both cerebral and muscular sy …
In two siblings with limb-girdle muscle weakness and episodic headaches and vomiting from early childhood, progressive neurologic deg …
"Clues on Balo's concentric sclerosis evolution from serial analysis of ADC values".
Ripellino P, Khonsari R, Stecco A, Filippi M, Perchinunno M, Cantello R. Ripellino P, et al. Int J Neurosci. 2016;126(1):88-95. doi: 10.3109/00207454.2014.989524. Epub 2015 Jan 5. Int J Neurosci. 2016. PMID: 25405537 Review.
Balo's sclerosis is considered a rare variant of multiple sclerosis characterized by demyelination with concentric rings. ...
Balo's sclerosis is considered a rare variant of multiple sclerosis characterized by demyelination with concentric rings. ...
Subacute sclerosing encephalitis.
Blattner RJ. Blattner RJ. J Pediatr. 1967 Dec;71(6):910-3. doi: 10.1016/s0022-3476(67)80023-4. J Pediatr. 1967. PMID: 4862504 Review. No abstract available.
113 results