Plasma homocysteine levels and folate status in children with sickle cell anemia.

PubWeight™: 3.27‹?› | Rank: Top 1%

🔗 View Article (PMID 10363855)

Published in J Pediatr Hematol Oncol on June 16, 1999

Authors

H M Rodriguez-Cortes1, J C Griener, K Hyland, T Bottiglieri, M J Bennett, B A Kamen, G R Buchanan

Author Affiliations

1: Department of Pediatrics, The University of Texas Southwestern Medical Center at Dallas Center for Cancer and Blood Disorders, 75235-9063, USA.

Articles by these authors

Potocytosis: sequestration and transport of small molecules by caveolae. Science (1992) 4.94

Cholesterol controls the clustering of the glycophospholipid-anchored membrane receptor for 5-methyltetrahydrofolate. J Cell Biol (1990) 4.37

AUX1 regulates root gravitropism in Arabidopsis by facilitating auxin uptake within root apical tissues. EMBO J (1999) 4.00

The glycophospholipid-linked folate receptor internalizes folate without entering the clathrin-coated pit endocytic pathway. J Cell Biol (1990) 3.96

The crystal structure of diphtheria toxin. Nature (1992) 3.80

Plasma beta-amyloid and white matter lesions in AD, MCI, and cerebral amyloid angiopathy. Neurology (2006) 3.68

Distribution of the folate receptor GP38 in normal and malignant cell lines and tissues. Cancer Res (1992) 3.66

Secondary acute myeloid leukemia in children with acute lymphoblastic leukemia treated with etoposide. J Clin Oncol (1993) 3.41

Comparative anatomy of the aldo-keto reductase superfamily. Biochem J (1997) 3.39

Bone marrow transplants from HLA-identical siblings as compared with chemotherapy for children with acute lymphoblastic leukemia in a second remission. N Engl J Med (1994) 3.26

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. Hum Mol Genet (1999) 3.22

High-dose intravenous methylprednisolone therapy for pain in children and adolescents with sickle cell disease. N Engl J Med (1994) 3.10

Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition. Hum Mol Genet (2001) 2.93

Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor. Cell (1998) 2.80

Enhancement of recovery from psychiatric illness by methylfolate. Lancet (1990) 2.73

AXR4 is required for localization of the auxin influx facilitator AUX1. Science (2006) 2.49

Severe bleeding events in adults and children with primary immune thrombocytopenia: a systematic review. J Thromb Haemost (2015) 2.46

Lowering the cholesterol content of MA104 cells inhibits receptor-mediated transport of folate. J Cell Biol (1992) 2.30

The effect of childbirth on pelvic organ mobility. Obstet Gynecol (2003) 2.29

Oligomer formation by 3D domain swapping: a model for protein assembly and misassembly. Adv Protein Chem (1997) 2.17

Ifosfamide: should the honeymoon be over? J Clin Oncol (1995) 2.13

Stable mixed hematopoietic chimerism after bone marrow transplantation for sickle cell anemia. Biol Blood Marrow Transplant (2001) 2.10

Antenatal screening in Oxford for fetal neural tube defects. Br J Obstet Gynaecol (1979) 2.06

The acute chest syndrome of sickle cell disease. J Pediatr (1999) 2.04

Protein kinase C activators inhibit receptor-mediated potocytosis by preventing internalization of caveolae. J Cell Biol (1994) 2.04

Receptor-mediated folate accumulation is regulated by the cellular folate content. Proc Natl Acad Sci U S A (1986) 1.95

Long term follow up of newborns tested with the auditory response cradle. Arch Dis Child (1984) 1.91

Fatty acid oxidation disorders: a new class of metabolic diseases. J Pediatr (1992) 1.85

Serotype-specific immunoglobulin G antibody responses to pneumococcal polysaccharide vaccine in children with sickle cell anemia: effects of continued penicillin prophylaxis. J Pediatr (1996) 1.84

Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development. Nat Genet (1999) 1.82

A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women. N Engl J Med (1999) 1.79

Predictive value of ultrasound measurement in early pregnancy: a randomized controlled trial. Br J Obstet Gynaecol (1982) 1.78

Major hemorrhage in children with idiopathic thrombocytopenic purpura: immediate response to therapy and long-term outcome. J Pediatr (1998) 1.77

Complementary DNA for the folate binding protein correctly predicts anchoring to the membrane by glycosyl-phosphatidylinositol. J Clin Invest (1989) 1.75

Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, Pennsylvania. Am J Med Genet (1991) 1.74

Comparison of laparoscopic and open splenectomy in children with hematologic disorders. J Pediatr (1997) 1.67

Novel auxin transport inhibitors phenocopy the auxin influx carrier mutation aux1. Plant J (2001) 1.67

Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. Am J Gastroenterol (1996) 1.66

A pilot study of outpatient management of febrile neutropenic children with cancer at low risk of bacteremia. J Pediatr (1996) 1.66

Cloning of a tumor-associated antigen: MOv18 and MOv19 antibodies recognize a folate-binding protein. Cancer Res (1991) 1.65

Central-nervous-system methyl-group metabolism in children with neurological complications of HIV infection. Lancet (1990) 1.64

Multiple sclerosis and macrocytosis. Acta Neurol Scand (1990) 1.64

Maternal serum-alpha-fetoprotein and low birth-weight. Lancet (1977) 1.64

Value of C-reactive protein determination in the initial diagnostic evaluation of the febrile, neutropenic child with cancer. Pediatr Infect Dis J (1992) 1.61

Bone pain as an initial symptom of childhood acute lymphoblastic leukemia: association with nearly normal hematologic indexes. J Pediatr (1990) 1.59

A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts. J Pediatr (1994) 1.59

The switch mechanism and the bipolar/unipolar dichotomy. Br J Psychiatry (1989) 1.58

Beneficial effect of intravenous dexamethasone in children with mild to moderately severe acute chest syndrome complicating sickle cell disease. Blood (1998) 1.57

Newly diagnosed idiopathic thrombocytopenic purpura in childhood: an observational study. Lancet (2002) 1.56

Tetrahydrobiopterin deficiency in human rabies. J Inherit Metab Dis (2008) 1.56

Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia. Proc Natl Acad Sci U S A (1975) 1.55

Aromatic L-amino acid decarboxylase deficiency: an extrapyramidal movement disorder with oculogyric crises. Eur J Paediatr Neurol (1997) 1.54

The changing epidemiology of bacteremia in neutropenic children with cancer. Pediatr Infect Dis J (1995) 1.52

Phase II investigational window using carboplatin, iproplatin, ifosfamide, and epirubicin in children with untreated disseminated neuroblastoma: a Pediatric Oncology Group study. J Clin Oncol (1994) 1.51

Catheter-related thrombosis in children with cancer. J Pediatr (2001) 1.51

Endothelial dysfunction and elevation of S-adenosylhomocysteine in cystathionine beta-synthase-deficient mice. Circ Res (2001) 1.50

Open study of the catechol-O-methyltransferase inhibitor tolcapone in major depressive disorder. J Clin Psychopharmacol (1999) 1.50

Intensive oral methotrexate protects against lymphoid marrow relapse in childhood B-precursor acute lymphoblastic leukemia. J Clin Oncol (1996) 1.50

Use of high-fat formula for premature infants with bronchopulmonary dysplasia: metabolic, pulmonary, and nutritional studies. J Pediatr (1994) 1.50

Multiple sclerosis and macrocytosis. Lancet (1989) 1.46

Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduria. Hum Mol Genet (1998) 1.46

The significance of subnormal serum vitamin B12 concentration in older people: a case control study. J Am Geriatr Soc (1996) 1.45

Malabsorption and defective utilization of iron in three siblings. J Pediatr (1981) 1.44

Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathways. Mol Genet Metab (2000) 1.44

Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death. J Clin Invest (2001) 1.43

Sjogren's syndrome. A case report with an additional diagnostic aid. Arch Intern Med (1966) 1.43

Ratio of methotrexate to folate uptake by lymphoblasts in children with B-lineage acute lymphoblastic leukemia: a pilot study. J Pediatr Hematol Oncol (2000) 1.41

Comparison of the interactions of transferrin receptor and transferrin receptor 2 with transferrin and the hereditary hemochromatosis protein HFE. J Biol Chem (2000) 1.41

Outpatient management of febrile illness in infants and young children with sickle cell anemia. J Pediatr (1990) 1.41

Mutational analysis of the transferrin receptor reveals overlapping HFE and transferrin binding sites. J Mol Biol (2001) 1.41

Therapeutic concepts in succinate semialdehyde dehydrogenase (SSADH; ALDH5a1) deficiency (gamma-hydroxybutyric aciduria). Hypotheses evolved from 25 years of patient evaluation, studies in Aldh5a1-/- mice and characterization of gamma-hydroxybutyric acid pharmacology. J Inherit Metab Dis (2007) 1.41

Implantable venous access devices in children with hemophilia: a report of low infection rates. J Pediatr (1998) 1.40

Subclavian cannulation with ultrasound: a novel method. Anaesthesia (2010) 1.39

Cellular localization of the folate receptor: potential role in drug toxicity and folate homeostasis. Cancer Res (1992) 1.38

The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy. Proc Natl Acad Sci U S A (1995) 1.38

4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolism. Neuropediatrics (1998) 1.37

The t(1;14)(p34;q11) is nonrandom and restricted to T-cell acute lymphoblastic leukemia: a Pediatric Oncology Group study. Blood (1990) 1.36

Cardiovascular risk factors in young adult survivors of childhood acute lymphoblastic leukemia. J Pediatr Hematol Oncol (2001) 1.35

Folate, vitamin B12, and homocysteine in major depressive disorder. Am J Psychiatry (1997) 1.35

Defects of metabolism of fatty acids in the sudden infant death syndrome. Br Med J (Clin Res Ed) (1985) 1.34

Subacute combined degeneration with high serum vitamin B12 level and abnormal vitamin B12 binding protein. New cause of an old syndrome. Arch Neurol (1993) 1.32

Clinical features and outcome of T-cell acute lymphoblastic leukemia in childhood with respect to alterations at the TAL1 locus: a Pediatric Oncology Group study. Blood (1993) 1.30

Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenase. Nat Genet (2001) 1.28

Discontinuing penicillin prophylaxis in children with sickle cell anemia. Prophylactic Penicillin Study II. J Pediatr (1995) 1.27

Association of homocysteine with plasma amyloid beta protein in aging and neurodegenerative disease. Neurology (2005) 1.26

Mild hyperhomocyst(e)inemia: a possible risk factor for cervical artery dissection. Stroke (2001) 1.25

Trials with the auditory response cradle. 1--Neonatal responses to auditory stimuli. Br J Audiol (1979) 1.25

Acute infarction of long bones in children with sickle cell anemia. J Pediatr (1982) 1.23

Severe hemolytic anemia in black children with glucose-6-phosphate dehydrogenase deficiency. Pediatrics (1982) 1.23

Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders. J Inherit Metab Dis (2000) 1.22

Neurological aspects of biopterin metabolism. Arch Dis Child (1986) 1.22

Childhood ITP: 12 months follow-up data from the prospective registry I of the Intercontinental Childhood ITP Study Group (ICIS). Pediatr Blood Cancer (2006) 1.21

Prevalence of priapism in children and adolescents with sickle cell anemia. J Pediatr Hematol Oncol (2000) 1.21

Grading of late effects in young adult survivors of childhood cancer followed in an ambulatory adult setting. Cancer (2000) 1.21

Fatal hemolysis induced by ceftriaxone in a child with sickle cell anemia. J Pediatr (1995) 1.21

Deficiency of medium chain fatty acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome. Br Med J (Clin Res Ed) (1984) 1.19

Programs for adult survivors of childhood cancer. J Clin Oncol (1998) 1.19

Cerebral folate deficiency with developmental delay, autism, and response to folinic acid. Neurology (2005) 1.18