Search Results - "Scheuerle, A. E."

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  1. 1

    Final results from the Betaseron (interferon β-1b) Pregnancy Registry: a prospective observational study of birth defects and pregnancy-related adverse events by Coyle, P K, Sinclair, S M, Scheuerle, A E, Thorp, J M, Albano, J D, Rametta, M J

    Published in BMJ open (01-01-2014)
    “…Objective Women with multiple sclerosis are often diagnosed and treated during their reproductive years. Limited data are available on the safety of treatment…”
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    Journal Article
  2. 2

    Selection Against Mutant Alleles in Blood Leukocytes is a Consistent Feature in Incontinentia Pigmenti Type 2 by Parrish, Julia E., Scheuerle, Angela E., Lewis, Richard A., Levy, Moise L., Nelson, David L.

    Published in Human molecular genetics (01-11-1996)
    “…Incontinentia Pigmenti 2 (IP2) is an X-linked dominant disorder with male lethality. Affected females display a characteristic skin eruption that evolves…”
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    Journal Article
  3. 3

    Frequency of prenatal diagnosis of birth defects in Houston, Galveston and the Lower Rio Grande Valley, Texas 1995 by Waller, D K, Pujazon, M A, Canfield, M A, Scheuerle, A E, Byrne, J L

    Published in Fetal diagnosis and therapy (01-11-2000)
    “…Estimates of the proportion of birth defects diagnosed before birth exist for only a few types of birth defects and for a few geographic regions in the United…”
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    Journal Article
  4. 4

    Prenatal diagnosis and cesarean section in a large, population-based birth defects registry by Case, A. P., Colpitts, L. R., Langlois, P. H., Scheuerle, A. E.

    “…Objective. To describe the patterns of cesarean section (CS) and vaginal delivery by type of birth defect and determine whether prenatal diagnosis predicts a…”
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    Arginase deficiency presenting as cerebral palsy by SCHEUERLE, A. E, MCVIE, R, BEAUDET, A. L, SHAPIRA, S. K

    Published in Pediatrics (Evanston) (01-05-1993)
    “…Arginase catalyzes the conversion of arginine to ornithine and urea in the final step of the urea cycle. The enzyme deficiency disease, argininemia, is a rare…”
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  7. 7

    Gonadal mosaicism for incontinentia pigmenti in a healthy male by Kirchman, T T, Levy, M L, Lewis, R A, Kanzler, M H, Nelson, D L, Scheuerle, A E

    Published in Journal of medical genetics (01-11-1995)
    “…Incontinentia pigmenti (IP) is a genodermatosis that segregates as an X linked dominant trait with male lethality. The disease has been linked to Xq28 in a…”
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    Journal Article
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    Male cases of incontinentia pigmenti: Case report and review by Scheuerle, Angela E.

    Published in American journal of medical genetics (18-05-1998)
    “…Male patients with Bloch‐Sulzberger incontinentia pigmenti (IP type II) are rare and more severely affected than their female counterparts, with a significant…”
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    Journal Article
  10. 10

    Do infants with major congenital anomalies have an excess of macrosomia? by Waller, D.K., Keddie, A.M., Canfield, M.A., Scheuerle, A.E.

    Published in Teratology (Philadelphia) (01-12-2001)
    “…Background Infants that develop congenital anomalies may also have an excess prevalence of macrosomia (birth weight ≥4,000 g). This may indicate that…”
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    Journal Article Conference Proceeding
  11. 11

    Pregnancy Outcomes After Exposure to Certolizumab Pegol: Updated Results From a Pharmacovigilance Safety Database by Clowse, Megan E B, Scheuerle, Angela E, Chambers, Christina, Afzali, Anita, Kimball, Alexa B, Cush, John J, Cooney, Maureen, Shaughnessy, Laura, Vanderkelen, Mark, Förger, Frauke

    Published in Arthritis & rheumatology (Hoboken, N.J.) (01-09-2018)
    “…Anti-tumor necrosis factor (anti-TNF) medications are effective in controlling chronic inflammatory diseases, but information about their use and safety in…”
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    Journal Article
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    Involvement of the thymus and cellular immune system in craniofacial malformation syndromes by Scheuerle, A E, Good, R A, Habal, M B

    Published in The Journal of craniofacial surgery (01-04-1990)
    “…Craniofacial structures, the aortic arch, thymus, and parathyroid glands all arise from the embryologic pharyngeal pouches, and DiGeorge and Job craniofacial…”
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    Journal Article
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