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

Year Number of Results
1946 3
1947 2
1948 3
1949 1
1950 2
1951 2
1952 7
1953 2
1954 2
1955 2
1956 1
1957 4
1958 3
1959 2
1960 3
1961 3
1962 4
1963 7
1964 8
1965 5
1966 12
1967 18
1968 19
1969 14
1970 13
1971 10
1972 19
1973 20
1974 16
1975 17
1976 17
1977 15
1978 20
1979 9
1980 15
1981 14
1982 11
1983 15
1984 9
1985 15
1986 11
1987 17
1988 11
1989 20
1990 25
1991 20
1992 30
1993 30
1994 37
1995 25
1996 31
1997 30
1998 24
1999 40
2000 39
2001 38
2002 40
2003 41
2004 43
2005 45
2006 54
2007 46
2008 46
2009 54
2010 60
2011 68
2012 62
2013 73
2014 64
2015 74
2016 83
2017 90
2018 85
2019 83
2020 126
2021 118
2022 115
2023 132
2024 51

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2,272 results

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Page 1
Hallervorden-Spatz Disease.
Bokhari MR, Zulfiqar H, Bokhari SRA. Bokhari MR, et al. 2023 Jul 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Jul 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 28613462 Free Books & Documents.
Hallervorden-Spatz disease, now more commonly known as pantothenate kinase-associated neurodegeneration (PKAN), is a rare autosomal recessive neurodegenerative disorder associated with iron accumulation in the brain nuclei and characterized by progressive extrapyramidal dy …
Hallervorden-Spatz disease, now more commonly known as pantothenate kinase-associated neurodegeneration (PKAN), is a rare autosomal r …
Hallervorden-Spatz syndrome.
Swaiman KF. Swaiman KF. Pediatr Neurol. 2001 Aug;25(2):102-8. doi: 10.1016/s0887-8994(01)00253-3. Pediatr Neurol. 2001. PMID: 11551740 Review.
The historic and current status of Hallervorden-Spatz syndrome diagnosis, classification, and therapies are discussed. ...The recent report of a defect in a novel pantothenate kinase gene (PANK2) in Hallervorden-Spatz syndrome will undoubtedly lead the way to future …
The historic and current status of Hallervorden-Spatz syndrome diagnosis, classification, and therapies are discussed. ...The recent …
Response.
Baroud S, Bazerbachi F, Abu Dayyeh BK. Baroud S, et al. Gastrointest Endosc. 2023 Nov;98(5):873-874. doi: 10.1016/j.gie.2023.07.002. Gastrointest Endosc. 2023. PMID: 37863574 No abstract available.
Tandem Breastfeeding.
Spatz DL. Spatz DL. MCN Am J Matern Child Nurs. 2023 Nov-Dec 01;48(6):343. doi: 10.1097/NMC.0000000000000958. MCN Am J Matern Child Nurs. 2023. PMID: 37840206 No abstract available.
A case of Hallervorden-Spatz disease presenting as catatonic schizophrenia.
Pawar Y, Kalra G, Sonavane S, Shah N. Pawar Y, et al. Indian J Psychiatry. 2013 Oct;55(4):386-9. doi: 10.4103/0019-5545.120553. Indian J Psychiatry. 2013. PMID: 24459313 Free PMC article.
Hallervorden-Spatz disease belongs to a group of disorders characterized by predominant involvement of basal ganglia. ...Very few cases of this disease have been reported from India. We report a case of Hallervorden-Spatz disease that presented to the psychiatry out …
Hallervorden-Spatz disease belongs to a group of disorders characterized by predominant involvement of basal ganglia. ...Very few cas …
Hallervorden-Spatz disease.
Dashti M, Chitsaz A. Dashti M, et al. Adv Biomed Res. 2014 Sep 12;3:191. doi: 10.4103/2277-9175.140623. eCollection 2014. Adv Biomed Res. 2014. PMID: 25317409 Free PMC article.
Hallervorden-Spatz disease (HSD) is a rare disorder characterized by progressive extrapyramidal dysfunction and dementia. Hallervorden and Spatz first described the disease, in 1922 as a form of familial brain degeneration characterized by iron deposition in the bra …
Hallervorden-Spatz disease (HSD) is a rare disorder characterized by progressive extrapyramidal dysfunction and dementia. Hallervorde …
Hallervorden spatz disease: MR and pathological findings of a rare case.
Sharma MC, Aggarwal N, Bihari M, Goyal V, Gaikwed S, Vaishya S, Sarkar C. Sharma MC, et al. Neurol India. 2005 Mar;53(1):102-4. Neurol India. 2005. PMID: 15805666 Free article. Review.
We describe a child with pathologically proven Hallervorden Spatz disease. He presented with extrapyramidal symptoms and characteristic "eye-of-the-tiger" sign on magnetic resonance imaging. ...
We describe a child with pathologically proven Hallervorden Spatz disease. He presented with extrapyramidal symptoms and characterist …
Marijuana and Breastfeeding.
Spatz DL. Spatz DL. MCN Am J Matern Child Nurs. 2022 Jan-Feb 01;47(1):54. doi: 10.1097/NMC.0000000000000784. MCN Am J Matern Child Nurs. 2022. PMID: 34860790 No abstract available.
Case of Hallervorden-Spatz Syndrome: A Tale of Twin Sisters.
Reddy N, Sharma J, Sharma A. Reddy N, et al. Neurol India. 2024 Mar 1;72(2):411-413. doi: 10.4103/ni.ni_1135_22. Epub 2024 Apr 30. Neurol India. 2024. PMID: 38691487 Free article.
Hallervorden-Spatz syndrome, now known as pantothenate kinase-associated neurodegeneration (PKAN), is a rare autosomal recessive disorder that is characterized by cerebral iron deposition and leads to progressive extrapyramidal dysfunction and dementia. ...
Hallervorden-Spatz syndrome, now known as pantothenate kinase-associated neurodegeneration (PKAN), is a rare autosomal recessive diso …
MR imaging in a case of Hallervorden-Spatz disease.
Tanfani G, Mascalchi M, Dal Pozzo GC, Taverni N, Saia A, Trevisan C. Tanfani G, et al. J Comput Assist Tomogr. 1987 Nov-Dec;11(6):1057-8. doi: 10.1097/00004728-198711000-00027. J Comput Assist Tomogr. 1987. PMID: 3680689
Magnetic resonance using a 0.5 T system and a T2-weighted spin-echo pulse sequence revealed symmetric areas of marked hypointensity of the globi pallidi in a case with a family history of and presenting with clinical features consistent with Hallervorden-Spatz disease. No …
Magnetic resonance using a 0.5 T system and a T2-weighted spin-echo pulse sequence revealed symmetric areas of marked hypointensity of the g …
2,272 results