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Items: 1 to 20 of 88

1.

A young child with seizures and mild developmental delay. Diagnosis: Alexander disease.

Seguias L, Khan M.

Pediatr Ann. 2013 Jun 1;42(6):234-7. doi: 10.3928/00904481-20130522-06. No abstract available.

PMID:
23718245
2.

A 2-month-old infant with vomiting, seizures, and progressive apathy.

Larsen A, Martin C, Meyer S, Rohrer T, Papanagiotou P, van der Knaap M, Gortner L.

Eur J Pediatr. 2012 Jun;171(6):993-5. doi: 10.1007/s00431-012-1681-0.

PMID:
22302460
3.

Early cerebral images of Alexander disease: report of one case.

Huang YT, Chen CC, Chiu PC, Lai PH, Hsieh KS.

Acta Paediatr Taiwan. 2004 Jan-Feb;45(1):52-5.

PMID:
15264709
4.

A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis.

Sakakibara T, Takahashi Y, Fukuda K, Inoue T, Kurosawa T, Nishikubo T, Shima M, Taoka T, Aida N, Tsujino S, Kanazawa N, Yoshioka A.

Brain Dev. 2007 Sep;29(8):525-8. Epub 2007 Mar 23.

PMID:
17383133
5.

INFANTILE ALEXANDER'S DISEASE: A CASE WITH CHARACTERISTIC MRI FEATURES.

Mazhar N, Saeed U.

J Ayub Med Coll Abbottabad. 2016 Jan-Mar;28(1):183-5.

PMID:
27323590
6.

A novel mutation in the GFAP gene in a familial adult onset Alexander disease.

Salmaggi A, Botturi A, Lamperti E, Grisoli M, Fischetto R, Ceccherini I, Caroli F, Boiardi A.

J Neurol. 2007 Sep;254(9):1278-80. Epub 2007 Aug 16. No abstract available.

PMID:
17703343
7.

Alexander disease as a cause of nocturnal vomiting in a 7-year-old girl.

Niinikoski H, Haataja L, Brander A, Valanne L, Blaser S.

Pediatr Radiol. 2009 Aug;39(8):872-5. doi: 10.1007/s00247-009-1289-3. Epub 2009 May 6.

PMID:
19418047
8.

Alexander disease with serial MRS and a new mutation in the glial fibrillary acidic protein gene.

Bassuk AG, Joshi A, Burton BK, Larsen MB, Burrowes DM, Stack C.

Neurology. 2003 Oct 14;61(7):1014-5. No abstract available.

PMID:
14557587
9.

Alexander disease with mild dorsal brainstem atrophy and infantile spasms.

Torisu H, Yoshikawa Y, Yamaguchi-Takada Y, Yano T, Sanefuji M, Ishizaki Y, Sawaishi Y, Hara T.

Brain Dev. 2013 May;35(5):441-4. doi: 10.1016/j.braindev.2012.06.009. Epub 2012 Jul 20.

PMID:
22818990
10.

Magnetic resonance imaging findings in Alexander disease.

Matarese CA, Renaud DL.

Pediatr Neurol. 2008 May;38(5):373-4. doi: 10.1016/j.pediatrneurol.2008.01.004. No abstract available.

PMID:
18410858
11.

[Clinical and genetic study of twelve Chinese patients with Alexander disease].

Zang LL, Wu Y, Wang JM, Gu Q, Jiang YW, Gao ZJ, Yang YL, Xiao JX, Wu XR.

Zhonghua Er Ke Za Zhi. 2012 May;50(5):371-5. Chinese.

PMID:
22883041
12.

Adult-onset Alexander disease with palatal myoclonus and intraventricular tumour.

Hirayama T, Fukae J, Noda K, Fujishima K, Yamamoto T, Mori K, Maeda M, Hattori N, Shiroma N, Tsurui S, Okuma Y.

Eur J Neurol. 2008 Feb;15(2):e16-7. doi: 10.1111/j.1468-1331.2007.02031.x. No abstract available.

PMID:
18217876
13.

Alexander disease: early presence of cerebral MRI criteria.

Poloni CB, Ferey S, Haenggeli CA, Delavelle J, Bottani A, Salomons GS, Van Der Knaap MS, Korff CM.

Eur J Paediatr Neurol. 2009 Nov;13(6):556-8. doi: 10.1016/j.ejpn.2008.11.008. Epub 2009 Jan 6.

PMID:
19128991
14.

A case of infantile Alexander disease accompanied by infantile spasms diagnosed by DNA analysis.

Lee JM, Kim AS, Lee SJ, Cho SM, Lee DS, Choi SM, Kim DK, Ki CS, Kim JW.

J Korean Med Sci. 2006 Oct;21(5):954-7.

15.

Alexander disease.

Zafeiriou DI, Dragoumi P, Vargiami E.

J Pediatr. 2013 Mar;162(3):648. doi: 10.1016/j.jpeds.2012.09.047. Epub 2012 Nov 10. No abstract available.

PMID:
23149175
16.

A woman in her 70s with chronic walking difficulties.

Fl√łnes IH, Haugarvoll K, Sundal C, Tzoulis C.

Tidsskr Nor Laegeforen. 2015 Oct 20;135(19):1753-5. doi: 10.4045/tidsskr.15.0111. eCollection 2015 Oct 20. English, Norwegian. No abstract available.

17.

A case of infantile Alexander disease with a milder phenotype and a novel GFAP mutation, L90P.

Suzuki Y, Kanazawa N, Takenaka J, Okumura A, Negoro T, Tsujino S.

Brain Dev. 2004 Apr;26(3):206-8.

PMID:
15030911
18.

Adult-onset Alexander disease with an R66Q mutation in GFAP presented with severe vocal cord paralysis during sleep.

Hida A, Ishiura H, Arai N, Fukuoka H, Hasuo K, Goto J, Uesaka Y, Tsuji S, Takeuchi S.

J Neurol. 2012 Oct;259(10):2234-6. doi: 10.1007/s00415-012-6540-4. Epub 2012 May 23. No abstract available.

PMID:
22619055
19.

An unusual presentation of juvenile Alexander disease.

Osorio MJ, Risen S, Alper G.

J Child Neurol. 2012 Apr;27(4):507-10. doi: 10.1177/0883073811419263. Epub 2011 Sep 21.

PMID:
21940697
20.

Incidental diagnosis of an asymptomatic adult-onset Alexander disease by brain magnetic resonance imaging for preoperative evaluation.

Sugiyama A, Sawai S, Ito S, Mukai H, Beppu M, Yoshida T, Kuwabara S.

J Neurol Sci. 2015 Jul 15;354(1-2):131-2. doi: 10.1016/j.jns.2015.05.001. Epub 2015 May 8. No abstract available.

PMID:
25982497

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