Facioscapulohumeral syndrome with cardiomyopathy.

PubWeight™: 0.81‹?›

🔗 View Article (PMC 2429785)

Published in Postgrad Med J on December 01, 1990

Authors

H Topaloğlu, A Celiker, S Ozme, S Göğüs, K Gücüyener, O O Erdinc, E Ozdirim

Articles by these authors

Double-chambered right ventricle: experience with 52 cases. Int J Cardiol (1995) 1.48

D2 receptor imaging with iodine-123-iodobenzamide brain SPECT in infants with hypoxic-ischemic brain injury. J Nucl Med (1998) 1.40

Initial experience with dual-sensor rate-responsive pacemakers in children. Eur Heart J (1996) 1.39

Partial anomalous pulmonary venous return. Evaluation of 51 cases. Jpn Heart J (1994) 1.30

Intracardiac thrombosis diagnosed by echocardiography in childhood: predisposing and etiological factors. Int J Cardiol (1993) 1.06

Myasthenic syndromes in Turkish kinships due to mutations in the acetylcholine receptor. Ann Neurol (1998) 0.98

Prednisolone therapy in Duchenne muscular dystrophy prolongs ambulation and prevents scoliosis. Eur J Neurol (2004) 0.96

Vogt-Koyanagi-Harada syndrome in siblings (with a brief review of the literature). Eur J Pediatr (1980) 0.96

Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature. Neuropediatrics (2002) 0.93

Chest pain in children referred to a cardiology clinic. Pediatr Cardiol (1995) 0.92

Cardiac lymphangioma. Am Heart J (1991) 0.92

Occidental type cerebromuscular dystrophy: a report of eleven cases. J Neurol Neurosurg Psychiatry (1991) 0.90

Cardiac hydatid cyst in a child: diagnostic value of echocardiography and magnetic resonance imaging. Acta Paediatr Jpn (1995) 0.89

Subacute sclerosing panencephalitis in Turkey: epidemiological features. J Trop Pediatr (1988) 0.88

Absent pulmonary valve syndrome with agenesis of the left pulmonary artery. Turk J Pediatr (1994) 0.88

Calpain-3 deficiency causes a mild muscular dystrophy in childhood. Neuropediatrics (1997) 0.87

Isolated noncompaction of ventricular myocardium. Cardiol Young (2001) 0.87

Improvement of myotonia with carbamazepine in three cases with the Schwartz-Jampel syndrome. Neuropediatrics (1993) 0.86

Cardiomyopathies in children. Clinical, epidemiological and prognostic evaluation. Jpn Heart J (1990) 0.85

Acute disseminated encephalomyelitis in childhood: report of 10 cases. J Child Neurol (1999) 0.85

Evaluation of bone mineral metabolism in children receiving carbamazepine and valproic acid. J Pediatr Endocrinol Metab (2000) 0.85

Comparison of sensitivity and specificity of tilt protocols with and without isoproterenol in children with unexplained syncope. Pacing Clin Electrophysiol (1997) 0.84

Clinical and genetic correlate in childhood onset Friedreich ataxia. Neuropediatrics (1999) 0.84

Head-up tilt test: a highly sensitive, specific test for children with unexplained syncope. Pediatr Cardiol (1997) 0.84

Tremor of tongue and dysarthria as the sole manifestation of Wilson's disease. Clin Neurol Neurosurg (1990) 0.84

Inappropriate sinus tachycardia following radiofrequency ablation of AV nodal tachycardia: incidence and clinical significance. Pacing Clin Electrophysiol (1994) 0.84

Neurinoma of the oculomotor nerve. Case report. J Clin Neuroophthalmol (1982) 0.83

A comparison between MUGA and echocardiography in patients with muscular dystrophy in the early detection of cardiac involvement. Pediatr Cardiol (1998) 0.83

MR imaging of pelvic and thigh muscles in congenital muscular dystrophy. Turk J Pediatr (2001) 0.83

Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci. Neuromuscul Disord (2000) 0.82

Heart rate variability in diabetic children: sensitivity of the time- and frequency-domain methods. Pediatr Cardiol (1993) 0.82

Suspected allergy to lamotrigine. Allergy (1999) 0.82

A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families. J Med Genet (2000) 0.81

Thrombosis in children with cardiac pathology: frequency of factor V Leiden and prothrombin G20210A mutations. Pediatr Cardiol (2003) 0.81

Evaluation by exercise testing of children with mild and moderate valvular aortic stenosis. Pediatr Int (2000) 0.81

Neurologic findings of vitamin B12 deficiency: presentation of 7 cases. Turk J Pediatr (1996) 0.81

Acute ascending myelitis and encephalopathy after intrathecal cytosine arabinoside and methotrexate in an adolescent boy with acute lymphoblastic leukemia. Brain Dev (1994) 0.81

Brain perfusion assessed by 99mTc-ECD SPECT imaging in pediatric patients with neurally mediated reflex syncope. Pacing Clin Electrophysiol (2005) 0.80

Dilatation of a restrictive interatrial communication using a balloon angioplasty catheter. Turk J Pediatr (2001) 0.80

HLA antigens in subacute sclerosing panencephalitis. Arch Neurol (1983) 0.80

Screening of deletions and RFLP analysis in Turkish DMD/BMD families by PCR. Clin Genet (1993) 0.80

Experience with propafenone for the treatment of cardiac arrhythmias in children. Turk J Pediatr (1991) 0.80

Adenosine induced torsades de pointes in a child with congenital long QT syndrome. Pacing Clin Electrophysiol (1994) 0.79

Intracranial calcification in children on computed tomography. Turk J Pediatr (1994) 0.79

Cimetidine as an immunomodulator in subacute sclerosing panencephalitis: a double blind, placebo-controlled study. Pediatr Infect Dis J (1993) 0.79

Medication-induced psychotic reaction. J Am Acad Child Adolesc Psychiatry (1997) 0.78

Prothrombin gene 20210 G-A mutation in Turkish patients with thrombosis. Am J Hematol (1998) 0.78

Ictal and interictal SPECT in a newborn infant with intractable seizure. Acta Paediatr (1997) 0.78

Causes of syncope in children: a prospective study. Int J Cardiol (1993) 0.78

3,4-diaminopyridine in childhood myasthenia: double-blind, placebo-controlled trial. J Child Neurol (1996) 0.78

Congenital sick sinus syndrome with breath holding and severe syncope episodes during infancy. A case report. Turk J Pediatr (2001) 0.78

Aortico-left ventricular tunnel. Thorac Cardiovasc Surg (1981) 0.78

[Unilateral paralysis of the abdominal wall musculature caused by thoracic intervertebral disk displacement]. Zentralbl Neurochir (1991) 0.78

Comparison of mid-term clinical experience with steroid-eluting active and passive fixation ventricular electrodes in children. Pacing Clin Electrophysiol (2000) 0.78

Mitochondrial deletion in a boy with growth hormone deficiency mimicking cerebral palsy. J Inherit Metab Dis (1998) 0.78

Association of xeroderma pigmentosum with thrombasthenia. Turk J Pediatr (1996) 0.78

Left ventricular structure and function by echocardiography in congenital muscular dystrophy. Brain Dev (1995) 0.78

Dermoid tumor with persistently low CSF glucose and unusual CT and MRI findings. Pediatr Neurol (1994) 0.78

Effectiveness and safety of intravenous amiodarone in drug-resistant tachyarrhythmias of children. Acta Paediatr Jpn (1998) 0.78

Analysis of 2017 Holter records in pediatric patients. Turk J Pediatr (2001) 0.77

Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families. Neuropediatrics (2001) 0.77

Beta-sarcoglycan gene mutations in Turkey. Acta Myol (2004) 0.77

Effect of carnitine supplementation on cardiac function in hemodialyzed children. Acta Paediatr Jpn (1998) 0.77

A comparative histopathologic and immunohistopathologic evaluation of cremaster muscles from boys with various inguinoscrotal pathologies. Eur J Pediatr Surg (2001) 0.77

Cutaneous anthrax. Cutis (1987) 0.77

Torsade de pointes associated with encephalitis. Turk J Pediatr (2000) 0.77

Peripheral neuropathy in a patient with D-2-hydroxyglutaric aciduria. J Inherit Metab Dis (2009) 0.77

Left ventricular structure and function by echocardiography in childhood swimmers. Jpn Heart J (1994) 0.77

Serum carnitine levels in newborns with perinatal asphyxia and relation to neurologic prognosis. Nutr Neurosci (2005) 0.77

Urinary nitric oxide in newborns with infections. Biol Neonate (2000) 0.77

Efficacy of transurethral electrovaporization of the prostate with respect to standard transurethral resection. J Endourol (1998) 0.77

Unusual variation of asplenia syndrome. Jpn Heart J (1991) 0.77

Short- and intermediate-term efficacy of amiodarone in infants and children with cardiac arrhythmia. Turk J Pediatr (1997) 0.76

Detection of Mycobacterium tuberculosis DNA in tissue samples of children with sarcoidosis. Pediatr Pulmonol (1997) 0.76

Moyamoya syndrome after radiation therapy for optic pathway glioma: case report. J Child Neurol (2000) 0.76

Abscess formation in posterior fossa dermoid cysts. Childs Nerv Syst (1997) 0.76

Frameshifting and splice-site mutations in the acetylcholine receptor epsilon subunit gene in three Turkish kinships with congenital myasthenic syndromes. Ann N Y Acad Sci (1998) 0.76

Role of excitatory aminoacids in neonatal hypoglycemia. Acta Paediatr Jpn (1998) 0.76

Selective involvement of the quadriceps muscle in congenital muscular dystrophies: an ultrasonographic study. Brain Dev (1992) 0.76

Heart disease in Friedreich's ataxia: a clinical and echocardiographic study. Acta Paediatr Jpn (1996) 0.76

Brain SPECT evaluation of patients with pure photosensitive epilepsy. J Nucl Med (1996) 0.76

Mitral and aortic insufficiency in polyarticular juvenile rheumatoid arthritis. Pediatr Cardiol (1994) 0.75

Sotalol in treatment of pediatric cardiac arrhythmias. Pediatr Int (2001) 0.75

MR angiography of left-sided cervical aortic arch with aberrant right subclavian artery. Br J Radiol (2007) 0.75

Evaluation of dysrhythmia in children with muscular dystrophy. Angiology (2000) 0.75

Allele distribution of D5S125, MAP1B5' and D5S679 microsatellite markers in Turkish spinal muscular atrophy families. Turk J Pediatr (1998) 0.75

Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations. Turk J Pediatr (2000) 0.75