Baraitser M - Search Results

1

Dominantly inherited congenital cerebellar ataxia with atrophy of the vermis.

Tomiwa K, Baraitser M, Wilson J. Tomiwa K, et al. Among authors: baraitser m. Pediatr Neurol. 1987 Nov-Dec;3(6):360-2. doi: 10.1016/0887-8994(87)90008-7. Pediatr Neurol. 1987. PMID: 3334022 Review.

2

Lethal congenital erythroderma: a newly recognised genetic disorder.

Shield JP, Judge MR, Reardon W, Baraitser M, Nohria M, Malone M, Harper JI. Shield JP, et al. Among authors: baraitser m. Clin Genet. 1992 May;41(5):273-7. doi: 10.1111/j.1399-0004.1992.tb03681.x. Clin Genet. 1992. PMID: 1535034

3

Distal spinal muscular atrophy with vocal cord paralysis.

Pridmore C, Baraitser M, Brett EM, Harding AE. Pridmore C, et al. Among authors: baraitser m. J Med Genet. 1992 Mar;29(3):197-9. doi: 10.1136/jmg.29.3.197. J Med Genet. 1992. PMID: 1552559 Free PMC article.

4

Autosomal recessive microcephaly with severe psychomotor retardation.

Scheffer IE, Baraitser M, Wilson J, Godfrey C, Brett EM. Scheffer IE, et al. Among authors: baraitser m. Neuropediatrics. 1992 Feb;23(1):53-6. doi: 10.1055/s-2008-1071313. Neuropediatrics. 1992. PMID: 1565220

5

Severe microcephaly associated with congenital varicella infection.

Scheffer IE, Baraitser M, Brett EM. Scheffer IE, et al. Among authors: baraitser m. Dev Med Child Neurol. 1991 Oct;33(10):916-20. doi: 10.1111/j.1469-8749.1991.tb14803.x. Dev Med Child Neurol. 1991. PMID: 1743417

6

Dominantly inherited syndrome comprising partially absent eye muscles, hydrocephaly, skeletal abnormalities, and a distinctive facial phenotype.

Chitty LS, McCrimmon R, Temple IK, Russell-Eggitt IM, Baraitser M. Chitty LS, et al. Among authors: baraitser m. Am J Med Genet. 1991 Sep 15;40(4):417-20. doi: 10.1002/ajmg.1320400407. Am J Med Genet. 1991. PMID: 1746603 No abstract available.

7

Autosomal dominant transmission of congenital erythroid hypoplastic anemia with radial abnormalities.

Hurst JA, Baraitser M, Wonke B. Hurst JA, et al. Among authors: baraitser m. Am J Med Genet. 1991 Sep 15;40(4):482-4. doi: 10.1002/ajmg.1320400422. Am J Med Genet. 1991. PMID: 1746615

8

Heterogeneity in dominant anterior segment malformations.

Holmström GE, Reardon WP, Baraitser M, Elston JS, Taylor DS. Holmström GE, et al. Among authors: baraitser m. Br J Ophthalmol. 1991 Oct;75(10):591-7. doi: 10.1136/bjo.75.10.591. Br J Ophthalmol. 1991. PMID: 1954207 Free PMC article.

9

Atypical facio-scapulo-humeral muscular dystrophy--a counselling dilemma.

Reardon W, Temple IK, Harwood G, Baraitser M. Reardon W, et al. Among authors: baraitser m. Clin Genet. 1991 Mar;39(3):172-7. doi: 10.1111/j.1399-0004.1991.tb03007.x. Clin Genet. 1991. PMID: 2036737

10

Megalencephaly with dysmyelination, spasticity, ataxia, seizures and distinctive neurophysiological findings in two siblings.

Harbord MG, Harden A, Harding B, Brett EM, Baraitser M. Harbord MG, et al. Among authors: baraitser m. Neuropediatrics. 1990 Aug;21(3):164-8. doi: 10.1055/s-2008-1071487. Neuropediatrics. 1990. PMID: 2234324

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