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Items: 1 to 20 of 172

1.

Congenital torticollis due to sternomastoid aplasia with unilateral cerebellar hypoplasia: a rare association.

Kumar VR, Sabapathy SR, Duraisami V.

Indian J Pediatr. 2012 Oct;79(10):1380-2. doi: 10.1007/s12098-011-0596-5. Epub 2011 Oct 14.

PMID:
21997867
2.

Congenital torticollis caused by unilateral absence of the sternocleidomastoid muscle.

Raman S, Takhtani D, Wallace EC.

Pediatr Radiol. 2009 Jan;39(1):77-9. doi: 10.1007/s00247-008-1021-8. Epub 2008 Oct 7.

PMID:
18839164
3.

Unilateral cerebellar aplasia.

Boltshauser E, Steinlin M, Martin E, Deonna T.

Neuropediatrics. 1996 Feb;27(1):50-3.

PMID:
8677027
4.

Congenital unilateral absence of sternocleidomastoid and trapezius muscles: a case report and literature review.

Vajramani A, Witham FM, Richards RH.

J Pediatr Orthop B. 2010 Sep;19(5):462-4. doi: 10.1097/BPB.0b013e32833ce404. Review.

PMID:
20647939
5.

[Congenital muscular torticollis due to sternocleidomastoid muscle aplasia].

Veselovskiĭ IuA.

Ortop Travmatol Protez. 1981 Jan;(1):49-50. Russian. No abstract available.

PMID:
7279397
7.

Lissencephaly with brainstem and cerebellar hypoplasia and congenital cataracts.

Abumansour IS, Wrogemann J, Chudley AE, Chodirker BN, Salman MS.

J Child Neurol. 2014 Jun;29(6):860-4. doi: 10.1177/0883073813485637. Epub 2013 Apr 26.

PMID:
23625088
8.

Congenital muscular torticollis: sequela of intrauterine or perinatal compartment syndrome.

Davids JR, Wenger DR, Mubarak SJ.

J Pediatr Orthop. 1993 Mar-Apr;13(2):141-7.

PMID:
8459000
9.

Cerebellar hypoplasia in a case with neurofibromatosis type 1.

Işikay S.

BMJ Case Rep. 2013 Dec 5;2013. pii: bcr2013202160. doi: 10.1136/bcr-2013-202160. No abstract available.

10.

Dominantly inherited nonprogressive cerebellar hypoplasia identified in utero.

Zerem A, Hacohen Y, Ben-Sira L, Lev D, Malinger G, Lerman-Sagie T.

J Child Neurol. 2012 Aug;27(8):1000-3. doi: 10.1177/0883073811431013. Epub 2012 Jan 12.

PMID:
22241708
11.

Clinical spectrum associated with cerebellar hypoplasia.

Wassmer E, Davies P, Whitehouse WP, Green SH.

Pediatr Neurol. 2003 May;28(5):347-51.

PMID:
12878295
12.

Dominantly inherited nonprogressive cerebellar hypoplasia identified in utero: no doubt.

Zerem A, Hacohen Y, Ben-Sira L, Lev D, Malinger G, Lerman-Sagie T.

J Child Neurol. 2013 Feb;28(2):279-80. doi: 10.1177/0883073812466292. No abstract available.

PMID:
23345527
13.

Torticollis due to a combination of sternomastoid contracture and congenital vertebral anomalies.

Brougham DI, Cole WG, Dickens DR, Menelaus MB.

J Bone Joint Surg Br. 1989 May;71(3):404-7.

14.
15.

Prenatal unilateral cerebellar hypoplasia diagnosed as PHACE syndrome.

Erturk O, Uygunoglu U, Celkan T, Yalcinkaya C.

Childs Nerv Syst. 2016 Apr;32(4):587-8. doi: 10.1007/s00381-016-3027-0. Epub 2016 Jan 29. No abstract available.

PMID:
26825811
16.

Congenital asymptomatic absence of unilateral sternocleidomastoid muscle.

Singh HP, Kumar S, Agarwal SP.

BMJ Case Rep. 2014 Jan 20;2014. pii: bcr2013202786. doi: 10.1136/bcr-2013-202786. No abstract available.

17.

Partial midline fusion of the cerebellar hemispheres with vertical folia: a new cerebellar malformation?

Takanashi J, Sugita K, Barkovich AJ, Takano H, Kohno Y.

AJNR Am J Neuroradiol. 1999 Jun-Jul;20(6):1151-3.

18.

Spectrum of neurodevelopmental disabilities in children with cerebellar malformations.

Bolduc ME, Du Plessis AJ, Sullivan N, Khwaja OS, Zhang X, Barnes K, Robertson RL, Limperopoulos C.

Dev Med Child Neurol. 2011 May;53(5):409-16. doi: 10.1111/j.1469-8749.2011.03929.x. Epub 2011 Mar 21.

19.

Verbal short-term memory and cerebellum: evidence from a patient with congenital cerebellar vermis hypoplasia.

Misciagna S, Iuvone L, Mariotti P, Silveri MC.

Neurocase. 2010 Apr;16(2):119-24. doi: 10.1080/13554790903329158. Epub 2009 Nov 18.

PMID:
19927261
20.

[Unilateral cerebellar hypoplasia: an alteration of vascular origin?].

Granados-Alzamora V, Pascual-Pascual SI, Pascual-Castroviejo I.

Rev Neurol. 2003 May 1-15;36(9):841-5. Spanish.

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