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A liquid chromatography/electrospray ionization mass spectrometry (LC–MS/MS) assay for the determination of irinotecan (CPT-11) and its two major metabolites in human liver microsomal incubations and human plasma samples

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2008-11, Vol.875 (2), p.522-530

2008

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Folic Acid for the Prevention of Neural Tube Defects

Pediatrics (Evanston), 1999-08, Vol.104 (2), p.325-327

Committee on Genetics

1999

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Cord Blood Banking for Potential Future Transplantation: Subject Review

Pediatrics (Evanston), 1999-07, Vol.104 (1), p.116-118

Work Group on Cord Blood Banking

1999

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Neonatal hyperbilirubinemia, phototherapy and risk of autism

Annals of epidemiology, 2005-09, Vol.15 (8), p.664-664

2005

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Survey of pediatrician practices in retrieving statewide authorized newborn screening results

Pediatrics (Evanston), 2001-08, Vol.108 (2), p.E22-e22

2001

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Molecular Genetic Testing in Pediatric Practice: A Subject Review

Pediatrics (Evanston), 2000-12, Vol.106 (6), p.1494-1497

Committee on Genetics

2000

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Newborn Screening for Congenital Hypothyroidism: Recommended Guidelines

Pediatrics (Evanston), 1993-06, Vol.91 (6), p.1203-1209

AAP Section on Endocrinology and Committee on Genetics, and American Thyroid Association Committee on Public Health

1993

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Health supervision for children with sickle cell disease

Pediatrics (Evanston), 2002-03, Vol.109 (3), p.526-535

2002

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Health Supervision for Children With Achondroplasia

Pediatrics (Evanston), 1995-03, Vol.95 (3), p.443-451

Committee on Genetics

1995

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Health Supervision for Children With Turner Syndrome

Pediatrics (Evanston), 1995-12, Vol.96 (6), p.1166-1173

Committee on Genetics

1995

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Health Supervision for Children With Down Syndrome

Pediatrics (Evanston), 1994-05, Vol.93 (5), p.855-859

Committee on Genetics

1994

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Health Supervision for Children With Fragile X Syndrome

Pediatrics (Evanston), 1996-08, Vol.98 (2), p.297-300

Committee on Genetics

1996

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Health Supervision for Children With Sickle Cell Diseases and Their Families

Pediatrics (Evanston), 1996-09, Vol.98 (3), p.467-472

Committee on Genetics

1996

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Prenatal Genetic Diagnosis for Pediatricians

Pediatrics (Evanston), 1994-06, Vol.93 (6), p.1010-1015

Committee on Genetics

1994

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Congenital diaphragmatic hernia and ipsilateral limb reduction defect: a new case, long-term follow-up and review of the literature

Clinical dysmorphology, 1997-07, Vol.6 (3), p.257-261

1997

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Newborn Screening Fact Sheets

Pediatrics (Evanston), 1996-09, Vol.98 (3), p.473-501

1996

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Partial trisomy 11q in a female infant with Robin sequence and congenital heart disease

The Cleft palate-craniofacial journal, 1992-01, Vol.29 (1), p.77-79

1992

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Umbilical cord hernia in a child with autosomal recessive chondrodysplasia punctata

Journal of medical genetics, 1986-02, Vol.23 (1), p.84-86

1986

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Prenatal testing and genetic counseling: physician's responsibility

Hospital progress, 1980-02, Vol.61 (2), p.8, 12

Desposito, F

1980

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Infants with cleft lip/cleft palate

Pediatrics in review, 1988-04, Vol.9 (10), p.331-334

1988

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Patient with a deletion of chromosome 21q and minimal phenotype

American journal of medical genetics, 2003-07, Vol.120A (1), p.142-143

2003

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Human Immunodeficiency Virus (HIV) Infection in Children

Hematology/oncology clinics of North America, 1987-09, Vol.1 (3), p.381-395

1987

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Unilateral calcification and contrast enhancement of the basal ganglia in a child with AIDS encephalopathy

American journal of neuroradiology : AJNR, 1987, Vol.8 (1), p.163-165

1987

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Comparative risks of amniocentesis and fetal blood sampling

Archives of disease in childhood, 1981-05, Vol.56 (5), p.405-405

1981

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79 T lymphocyte regulation of erythroid colonies in sickle cell anemia

Journal of allergy and clinical immunology, 1983, Vol.71 (1), p.108-108

1983

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A liquid chromatography/electrospray ionization mass spectrometry (LC–MS/MS) assay for the determination of irinotecan (CPT-11) and its two major metabolites in human liver microsomal incubations and human plasma samples

Folic Acid for the Prevention of Neural Tube Defects

Cord Blood Banking for Potential Future Transplantation: Subject Review

Neonatal hyperbilirubinemia, phototherapy and risk of autism

Survey of pediatrician practices in retrieving statewide authorized newborn screening results

Molecular Genetic Testing in Pediatric Practice: A Subject Review

Newborn Screening for Congenital Hypothyroidism: Recommended Guidelines

Health supervision for children with sickle cell disease

Health Supervision for Children With Achondroplasia

Health Supervision for Children With Turner Syndrome

Health Supervision for Children With Down Syndrome

Health Supervision for Children With Fragile X Syndrome

Health Supervision for Children With Sickle Cell Diseases and Their Families

Prenatal Genetic Diagnosis for Pediatricians

Congenital diaphragmatic hernia and ipsilateral limb reduction defect: a new case, long-term follow-up and review of the literature

Newborn Screening Fact Sheets

Partial trisomy 11q in a female infant with Robin sequence and congenital heart disease

Umbilical cord hernia in a child with autosomal recessive chondrodysplasia punctata

Prenatal testing and genetic counseling: physician's responsibility

Infants with cleft lip/cleft palate

Patient with a deletion of chromosome 21q and minimal phenotype

Human Immunodeficiency Virus (HIV) Infection in Children

Unilateral calcification and contrast enhancement of the basal ganglia in a child with AIDS encephalopathy

Comparative risks of amniocentesis and fetal blood sampling

79 T lymphocyte regulation of erythroid colonies in sickle cell anemia

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