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P.020 The North American AED Pregnancy Registry: A Canadian Subgroup Analysis (1997-2019)

Canadian journal of neurological sciences, 2021-11, Vol.48 (s3), p.S25-S25

2021

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Levetiracetam Pregnancy Registry: Final results and a review of the impact of registry methodology and definitions on the prevalence of major congenital malformations

Birth defects research, 2019-08, Vol.111 (13), p.872-887

2019

Volltextzugriff (PDF)

Limb deficiencies in newborn infants

Pediatrics (Evanston), 2001-10, Vol.108 (4), p.E64

2001

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Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): A possible locus for Fryns syndrome

American journal of medical genetics. Part A, 2006-01, Vol.140A (1), p.17-23

2006

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Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society

Hormone research, 2002, Vol.58 (4), p.188-195

2002

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Laterality defects in conjoined twins

Nature (London), 1996-11, Vol.384 (6607), p.321-321

1996

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Amniotic bands and exocelomic stickiness: Reply to Dr. Shepard

Birth defects research. A Clinical and molecular teratology, 2004-03, Vol.70 (3), p.154-154

Holmes, Lewis B.

2004

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Malformations Due to Presumed Spontaneous Mutations in Newborn Infants

The New England journal of medicine, 1989-01, Vol.320 (1), p.19-23

1989

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Congenital microcephaly: Phenotypic features in a consecutive sample of newborn infants

The Journal of pediatrics, 2001-08, Vol.139 (2), p.210-214

2001

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Trends in Congenital Malformations, 1974–1999: Effect of Prenatal Diagnosis and Elective Termination: Reply

Obstetrics and gynecology (New York. 1953), 2005-04, Vol.105 (4), p.903

2005

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Crossed Random Effect Models for Multiple Outcomes in a Study of Teratogenesis

Journal of the American Statistical Association, 2001-12, Vol.96 (456), p.1194-1204

2001

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Concern about Piracetam treatment for children with Down syndrome

Pediatrics (Evanston), 1999-05, Vol.103 (5 Pt 1), p.1078

Holmes, L B

1999

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Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): A possible locus for Fryns syndrome (Am J Med Genet 140A:17-23, 2006)

American journal of medical genetics. Part A, 2006-05, Vol.140A (9), p.1031-1031

2006

Volltextzugriff (PDF)

Topical tretinoin: photodamage treatment overview and developmental toxicology studies. Introduction

Journal of the American Academy of Dermatology, 1997-03, Vol.36 (3 Pt 2), p.S25

1997

Volltextzugriff (PDF)

Homeobox genes and congenital malformations

Laboratory investigation, 1992-06, Vol.66 (6), p.659

1992

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Head Circumference Standards in Neonates

Journal of child neurology, 1994-01, Vol.9 (1), p.63-66

1994

Volltextzugriff (PDF)

Mutations in human TBX3 alter limb, apocrine, and genital development in ulnar-mammary syndrome

Nature genetics, 1998-05, Vol.19 (1), p.102-102

1998

Volltextzugriff (PDF)

The diabetes in early pregnancy study : changes in cholesterol, triglycerides, body weight, and blood pressure

American journal of obstetrics and gynecology, 1992-02, Vol.166 (2), p.513-518

1992

Volltextzugriff (PDF)

Chorionic villus sampling and limb defects

Progress in clinical and biological research, 1993, Vol.383A, p.409

Holmes, L B

1993

Volltextzugriff (PDF)

2001 Teratogen Update Workshop summaries: Introduction

Teratology (Philadelphia), 2002-05, Vol.65 (5), p.199-199

Holmes, Lewis B.

2002

Volltextzugriff (PDF)

Etiologic Heterogeneity of Neural-Tube Defects

The New England journal of medicine, 1976-02, Vol.294 (7), p.365-369

1976

Volltextzugriff (PDF)

On the Use of Anencephalic Infants as Organ Donors

The New England journal of medicine, 1989-08, Vol.321 (6), p.391-393

1989

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Birthmarks with serious medical significance: Nevocellular nevi, sebaceous nevi, and multiple café au lait spots

The Journal of pediatrics, 1979-01, Vol.95 (5), p.696-700

1979

Volltextzugriff (PDF)

New editor's perspective

Teratology (Philadelphia), 1998-02, Vol.57 (2), p.i-i

Holmes, Lewis B.

1998

Volltextzugriff (PDF)

The syndrome of multiple ankyloses and facial anomalies. A neuropathologic analysis

Acta neuropathologica, 1980, Vol.50 (3), p.175-179

1980

Volltextzugriff (PDF)

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P.020 The North American AED Pregnancy Registry: A Canadian Subgroup Analysis (1997-2019)

Levetiracetam Pregnancy Registry: Final results and a review of the impact of registry methodology and definitions on the prevalence of major congenital malformations

Limb deficiencies in newborn infants

Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): A possible locus for Fryns syndrome

Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society

Laterality defects in conjoined twins

Amniotic bands and exocelomic stickiness: Reply to Dr. Shepard

Malformations Due to Presumed Spontaneous Mutations in Newborn Infants

Congenital microcephaly: Phenotypic features in a consecutive sample of newborn infants

Trends in Congenital Malformations, 1974–1999: Effect of Prenatal Diagnosis and Elective Termination: Reply

Crossed Random Effect Models for Multiple Outcomes in a Study of Teratogenesis

Concern about Piracetam treatment for children with Down syndrome

Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): A possible locus for Fryns syndrome (Am J Med Genet 140A:17-23, 2006)

Topical tretinoin: photodamage treatment overview and developmental toxicology studies. Introduction

Homeobox genes and congenital malformations

Head Circumference Standards in Neonates

Mutations in human TBX3 alter limb, apocrine, and genital development in ulnar-mammary syndrome

The diabetes in early pregnancy study : changes in cholesterol, triglycerides, body weight, and blood pressure

Chorionic villus sampling and limb defects

2001 Teratogen Update Workshop summaries: Introduction

Etiologic Heterogeneity of Neural-Tube Defects

On the Use of Anencephalic Infants as Organ Donors

Birthmarks with serious medical significance: Nevocellular nevi, sebaceous nevi, and multiple café au lait spots

New editor's perspective

The syndrome of multiple ankyloses and facial anomalies. A neuropathologic analysis

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