Acrocallosal Syndrome [majr:noexp] - Search Results

Year	Number of Results
2008	9
2009	19
2010	15
2011	8
2012	3
2013	2
2015	3
2018	1
2019	4
2024	0

1

Acrocallosal syndrome: a case report and literature survey.

Hodgson BD, Davies L, Gonzalez CD. Hodgson BD, et al. J Dent Child (Chic). 2009 May-Aug;76(2):170-7. J Dent Child (Chic). 2009. PMID: 19619433 Review.

2

Olfactory bulb and olfactory tract abnormalities in acrocallosal syndrome and Greig cephalopolysyndactyly syndrome.

Subramanian S, Soundara Rajan D, Gaesser J, Wen-Ya Lo C, Panigrahy A. Subramanian S, et al. Pediatr Radiol. 2019 Sep;49(10):1368-1373. doi: 10.1007/s00247-019-04480-8. Epub 2019 Aug 9. Pediatr Radiol. 2019. PMID: 31399769 Free PMC article.

3

MOLAR TOOTH SIGN AND ACROCALLOSAL SYNDROME--A REPORT ON A POLISH FAMILY AND REVIEW OF KIF7 SYNDROMOLOGY.

Krajewska-Walasek M, Kugaudo M, Jędrzejowska M, Cieślikowska A, Ichkou A, Attié-Bitach T, Jezela-Stanek A. Krajewska-Walasek M, et al. Genet Couns. 2015;26(2):171-9. Genet Couns. 2015. PMID: 26349186 Review.

4

Altered GLI3 and FGF8 signaling underlies acrocallosal syndrome phenotypes in Kif7 depleted mice.

Putoux A, Baas D, Paschaki M, Morlé L, Maire C, Attié-Bitach T, Thomas S, Durand B. Putoux A, et al. Hum Mol Genet. 2019 Mar 15;28(6):877-887. doi: 10.1093/hmg/ddy392. Hum Mol Genet. 2019. PMID: 30445565

5

Acrocallosal syndrome in a young hypertensive male.

Ramteke VV, Darole PA, Shaikh ZF, Padwal NJ, Agrawal B, Shrivastava MS, Kamath S. Ramteke VV, et al. BMJ Case Rep. 2011 May 3;2011:bcr1220103648. doi: 10.1136/bcr.12.2010.3648. BMJ Case Rep. 2011. PMID: 22696705 Free PMC article.

6

Acrocallosal Syndrome First Presenting with Acute Lymphoblastic Leukemia: A Rare Case Report.

Koker SA, Hazan F, Oymak Y, Soydan E, Karapınar TH, Ay Y, Demirağ B, Vergin RC. Koker SA, et al. Neurol India. 2019 Sep-Oct;67(5):1386-1387. doi: 10.4103/0028-3886.271244. Neurol India. 2019. PMID: 31744987 Free article. No abstract available.

7

A novel KIF7 mutation in two affected siblings with acrocallosal syndrome.

Karaer K, Yuksel Z, Ichkou A, Calisir C, Attié-Bitach T. Karaer K, et al. Clin Dysmorphol. 2015 Apr;24(2):61-4. doi: 10.1097/MCD.0000000000000080. Clin Dysmorphol. 2015. PMID: 25714560

8

A de novo GLI3 mutation in a patient with acrocallosal syndrome.

Speksnijder L, Cohen-Overbeek TE, Knapen MF, Lunshof SM, Hoogeboom AJ, van den Ouwenland AM, de Coo IF, Lequin MH, Bolz HJ, Bergmann C, Biesecker LG, Willems PJ, Wessels MW. Speksnijder L, et al. Am J Med Genet A. 2013 Jun;161A(6):1394-400. doi: 10.1002/ajmg.a.35874. Epub 2013 Apr 30. Am J Med Genet A. 2013. PMID: 23633388

9

Novel KIF7 mutations extend the phenotypic spectrum of acrocallosal syndrome.

Putoux A, Nampoothiri S, Laurent N, Cormier-Daire V, Beales PL, Schinzel A, Bartholdi D, Alby C, Thomas S, Elkhartoufi N, Ichkou A, Litzler J, Munnich A, Encha-Razavi F, Kannan R, Faivre L, Boddaert N, Rauch A, Vekemans M, Attié-Bitach T. Putoux A, et al. J Med Genet. 2012 Nov;49(11):713-20. doi: 10.1136/jmedgenet-2012-101016. J Med Genet. 2012. PMID: 23125460

10

Corpus callosum agenesis and rehabilitative treatment.

Chiappedi M, Bejor M. Chiappedi M, et al. Ital J Pediatr. 2010 Sep 17;36:64. doi: 10.1186/1824-7288-36-64. Ital J Pediatr. 2010. PMID: 20849621 Free PMC article. Review.

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