Limb-girdle muscular dystrophy: clinical manifest... [Pediatrics. 1968] - PubMed

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Limb-girdle musclar dystrophy: its larger significance. [Pediatrics. 1968]
Limb-girdle musclar dystrophy: its larger significance.
. Pediatrics. 1968 Feb; 41(2):382-4.
Poikiloderma atrophicans vasculare associated with muscular dystrophy. [Arch Dermatol. 1973]
Poikiloderma atrophicans vasculare associated with muscular dystrophy.
Woolfson H, McQueen A. Arch Dermatol. 1973 Jan; 107(1):115-7.
The incidence of lobulated fibres in the facioscapulo-humeral type of muscular dystrophy and the limb-girdle syndrome. [J Neurol Sci. 1973]
The incidence of lobulated fibres in the facioscapulo-humeral type of muscular dystrophy and the limb-girdle syndrome.
Bethlem J, van Wijngaarden GK, de Jong J. J Neurol Sci. 1973 Mar; 18(3):351-8.
Review Muscular dystrophy in childhood. [Dev Med Child Neurol. 1974]
Review Muscular dystrophy in childhood.
Moosa A. Dev Med Child Neurol. 1974 Feb; 16(1):97-111.
Review Limb girdle muscular dystrophy: reappraisal of a rejected entity. [Clin Neurol Neurosurg. 1994]
Review Limb girdle muscular dystrophy: reappraisal of a rejected entity.
van der Kooi AJ, de Visser M, Barth PG. Clin Neurol Neurosurg. 1994 Aug; 96(3):209-18.

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Cited by 9 PubMed Central articles

Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7. [Am J Hum Genet. 1999]
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.
Speer MC, Vance JM, Grubber JM, Lennon Graham F, Stajich JM, Viles KD, Rogala A, McMichael R, Chutkow J, Goldsmith C, et al. Am J Hum Genet. 1999 Feb; 64(2):556-62.
DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear gene. [Am J Hum Genet. 1997]
DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear gene.
Pratt VM, Jackson CE, Wallace DC, Gurley DS, Feit A, Feldman GL. Am J Hum Genet. 1997 Jul; 61(1):231-3.
Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy. [Am J Hum Genet. 1995]
Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.
Speer MC, Gilchrist JM, Chutkow JG, McMichael R, Westbrook CA, Stajich JM, Jorgenson EM, Gaskell PC, Rosi BL, Ramesar R. Am J Hum Genet. 1995 Dec; 57(6):1371-6.

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Limb-girdle muscular dystrophy: clinical manifestations and detection of preclin...
Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.
Pediatrics. 1968 Feb ;41(2):495-502.

PubMed
A comparison of maximum inspiratory and expiratory flow in health and in lung di...
A comparison of maximum inspiratory and expiratory flow in health and in lung disease.
Thorax. 1968 Jan ;23(1):38-45.

PubMed
Hb Potomac (101 Glu replaced by Asp): speculations on placental oxygen transport...
Hb Potomac (101 Glu replaced by Asp): speculations on placental oxygen transport in carriers of high-affinity hemoglobins.
Blood. 1978 Feb ;51(2):331-8.

PubMed
The first lie.
The first lie.
Psychiatry. 1968 Feb ;31(1):61-8.

PubMed
Structural characterization of hemoglobin-N-Seattle.
Structural characterization of hemoglobin-N-Seattle.
Biochim Biophys Acta. 1968 Feb 19 ;154(2):278-83.

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