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Results: 1 to 20 of 103

Similar articles for PubMed (Select 3527442)

1.

Segregation analysis of migraine in 128 families.

Devoto M, Lozito A, Staffa G, D'Alessandro R, Sacquegna T, Romeo G.

Cephalalgia. 1986 Jun;6(2):101-5.

PMID:
3527442
2.

Testing models for genetic determination in migraine.

Mochi M, Sangiorgi S, Cortelli P, Carelli V, Scapoli C, Crisci M, Monari L, Pierangeli G, Montagna P.

Cephalalgia. 1993 Dec;13(6):389-94.

PMID:
8313452
3.

A family with hemiplegic migraine and focal seizures.

Kramer U, Lerman-Sagi T, Margalith D, Harel S.

Eur J Paediatr Neurol. 1997;1(1):35-8.

PMID:
10728190
4.

Analysis of 31 families with an apparently autosomal-dominant transmission of migraine with aura in the nuclear family.

Ulrich V, Russell MB, Ostergaard S, Olesen J.

Am J Med Genet. 1997 Jul 25;74(4):395-7.

PMID:
9259375
5.

[Pedigree study of pathological myopia].

Yu ZQ, Fu CW, Shen FM, Chu RY.

Yi Chuan Xue Bao. 2005 Feb;32(2):130-5. Chinese.

PMID:
15759859
6.

Migraine: sex-influenced trait model?

Wang XP, Liu JM, Zhao YB.

Med Hypotheses. 2008;71(1):14-21. doi: 10.1016/j.mehy.2007.12.015. Epub 2008 Mar 4.

PMID:
18289799
7.

Migraine without aura and migraine with aura are inherited disorders.

Russell MB, Iselius L, Olesen J.

Cephalalgia. 1996 Aug;16(5):305-9.

PMID:
8869764
8.

Identification of an autosomal recessive mode of inheritance in paediatric Behçet's families by segregation analysis.

Molinari N, Koné Paut I, Manna R, Demaille J, Daures JP, Touitou I.

Am J Med Genet A. 2003 Oct 1;122A(2):115-8.

PMID:
12955762
9.

Cluster headache is an autosomal dominantly inherited disorder in some families: a complex segregation analysis.

Russell MB, Andersson PG, Thomsen LL, Iselius L.

J Med Genet. 1995 Dec;32(12):954-6.

10.
11.

[Genetics of migraine].

Evers S, Wieser T, Ringelstein EB.

Nervenarzt. 1996 Oct;67(10):837-45. Review. German.

PMID:
9036357
12.

Genetic heterogeneity of inherited cerebral cavernous malformation.

Günel M, Awad IA, Finberg K, Steinberg GK, Craig HD, Cepeda O, Nelson-Williams C, Lifton RP.

Neurosurgery. 1996 Jun;38(6):1265-71.

PMID:
8727164
13.

Genetic heterogeneity of familial hemiplegic migraine.

Ophoff RA, van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CP, Haan J, Lindhout D, Ferrari MD, Frants RR.

Genomics. 1994 Jul 1;22(1):21-6.

PMID:
7959770
14.

New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature.

Vérin M, Rolland Y, Landgraf F, Chabriat H, Bompais B, Michel A, Vahedi K, Martinet JP, Tournier-Lasserve E, Lemaitre MH, et al.

J Neurol Neurosurg Psychiatry. 1995 Dec;59(6):579-85.

15.

A genetic analysis of retinitis pigmentosa.

Boughman JA, Fishman GA.

Br J Ophthalmol. 1983 Jul;67(7):449-54.

16.

The inheritance of migraine with aura estimated by means of structural equation modelling.

Ulrich V, Gervil M, Kyvik KO, Olesen J, Russell MB.

J Med Genet. 1999 Mar;36(3):225-7.

17.

[Molecular genetics of migraine].

Tournier-Lasserve E.

Rev Neurol (Paris). 2005 Jul;161(6-7):651-3. Review. French.

PMID:
16141949
18.

Migraine with aura and white matter abnormalities: Notch3 mutation.

Ceroni M, Poloni TE, Tonietti S, Fabozzi D, Uggetti C, Frediani F, Simonetti F, Malaspina A, Alimonti D, Celano M, Ferrari M, Carrera P.

Neurology. 2000 May 9;54(9):1869-71.

PMID:
10802804
19.

[Clinico-genetic aspects of the ovarian failure syndrome].

Kirillova EA, Smetnik VP.

Tsitol Genet. 1992 May-Jun;26(3):56-62. Russian.

PMID:
1502734
20.

Segregation analysis of prostate cancer in France: evidence for autosomal dominant inheritance and residual brother-brother dependence.

Valeri A, Briollais L, Azzouzi R, Fournier G, Mangin P, Berthon P, Cussenot O, Demenais F.

Ann Hum Genet. 2003 Mar;67(Pt 2):125-37.

PMID:
12675688
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