Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Hanah Nasri"'
Publikováno v:
Birth Defects Res
Background To determine the frequency of malformations that would be identified in the limited surface examination of a newborn by the delivering nurse midwife in a resource-limited setting. Methods The limited surface examination will identify visib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1019900a84f74a192092dd0fcc853ece
https://doi.org/10.1002/bdr2.1887
https://doi.org/10.1002/bdr2.1887
Autor:
Lewis B. Holmes, Hanah Nasri
Publikováno v:
Birth defects researchREFERENCES. 113(13)
Background A terminal transverse limb defect with absence of the forearm and hand or just the hand is an uncommon limb deformity in an otherwise healthy newborn. Most of the affected infants also have tiny digit-like nubbins on the stump of the affec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8afb0e8515016bccec6b9eaf28fa5936
https://pubmed.ncbi.nlm.nih.gov/34240582
https://pubmed.ncbi.nlm.nih.gov/34240582
Publikováno v:
Birth Defects Research. 110:108-113
Background Infants of diabetic mothers have been shown in several studies to have an increased frequency of malformations. In previous studies, an increased frequency of several specific malformations has been noted, including anencephaly, bilateral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93ec5e9a5506fcfab8220091bb4a7316
https://doi.org/10.1002/bdr2.1155
https://doi.org/10.1002/bdr2.1155
Publikováno v:
Birth Defects Research. 110:148-156
Background Malformations surveillance programs have been carried out in consecutive populations of newborn infants at single hospitals, as well as in several hospitals in defined populations. A surveillance program begins with the review of the findi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c9abd4983d5f7a24b783d753fb71987
https://doi.org/10.1002/bdr2.1156
https://doi.org/10.1002/bdr2.1156
Publikováno v:
Birth Defects Research. 110:134-141
Background Postaxial polydactyly, type B is the most common type of polydactyly. The vestigial sixth finger is attached by a narrow neurovascular pedicle to the lateral aspect of the hand or foot at the level of the metacarpal-phalangeal joint or the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5c9d9e0d55deddd791a89db64ec67cc
https://doi.org/10.1002/bdr2.1184
https://doi.org/10.1002/bdr2.1184
Publikováno v:
Birth Defects Research. 110:98-107
Background Several malformations have been attributed to the process of vascular disruption. The central hypothesis for this etiology is that blood flow to a structure has been altered after that structure had formed normally. The decreased blood flo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e925431fda6047532232ff833714dc5
https://doi.org/10.1002/bdr2.1160
https://doi.org/10.1002/bdr2.1160
Autor:
Anne-Therese Hunt, Marie-Noel Westgate, Rebecca S. Beroukhim, Lewis B. Holmes, M Hassan Toufaily, Hanah Nasri, Drucilla J. Roberts
Publikováno v:
Birth Defects Research. 110:114-121
Background Stillbirth, defined as death of a fetus in utero after 20 weeks of gestation, occurs in 1 to 2% of pregnancies in the United States. Many of these stillborn infants have associated malformations, including chromosome abnormalities, neural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3376c794d0b073d5ac47fd9d8bb936b
https://doi.org/10.1002/bdr2.1097
https://doi.org/10.1002/bdr2.1097
Publikováno v:
Birth Defects Research. 110:92-97
Background The number of malformations attributed to mutations with autosomal or X-linked patterns of inheritance has increased steadily since the cataloging began in the 1960s. These diagnoses have been based primarily on the pattern of phenotypic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::254f52434921bbdcafabf34e36819323
https://doi.org/10.1002/bdr2.1101
https://doi.org/10.1002/bdr2.1101
Autor:
Christopher J. Stodgell, Jane Adams, Curtis K. Deutsch, Margaret L. Bauman, Rachel Stadelmaier, Hanah Nasri, Anne Hunt, Lewis B. Holmes
Publikováno v:
Birth Defects Research. 109:1134-1143
Background Valproic acid (VPA) is the most teratogenic anticonvulsant drug in clinical use today. Children exposed prenatally to VPA have previously been shown to have dysmorphic craniofacial features, identified subjectively but not by anthropometri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::598cfc2b48b9af81c30f3597ac4ffd6e
https://doi.org/10.1002/bdr2.1052
https://doi.org/10.1002/bdr2.1052
Publikováno v:
Birth defects research. 110(2)
The number of malformations attributed to mutations with autosomal or X-linked patterns of inheritance has increased steadily since the cataloging began in the 1960s. These diagnoses have been based primarily on the pattern of phenotypic features amo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::51ee46538524f8ddc4bc4ce2077233b4
https://pubmed.ncbi.nlm.nih.gov/29377642
https://pubmed.ncbi.nlm.nih.gov/29377642