Zobrazeno 1 - 10
of 34
pro vyhledávání: '"M T Mennuti"'
Autor:
M T, Mennuti
Publikováno v:
Obstetrics and gynecology. 98(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e618e3cc4ae5d8c3fd253b337e0c5150
https://pubmed.ncbi.nlm.nih.gov/11576562
https://pubmed.ncbi.nlm.nih.gov/11576562
Publikováno v:
American journal of medical genetics. 94(2)
We describe monozygotic twins with partially discordant phenotypes who were found to have a duplication of chromosome region 4q28.3-qter. The duplicated region of chromosome 4 resulted from an unbalanced segregation of a balanced maternal (4;22)(q28.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::34c5b8a5cda4c08d8c467ccab4a9d121
https://pubmed.ncbi.nlm.nih.gov/10982969
https://pubmed.ncbi.nlm.nih.gov/10982969
Publikováno v:
Archives of pathologylaboratory medicine. 121(7)
Neuroblastoma, a tumor of primitive neuroectodermal cells, is one of the most common solid malignancies of neonates. Placental metastases have been described in rare cases of congenital neuroblastoma, usually in association with hydrops fetalis, plac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::467cbb07bf84269a68429980e05af5cf
https://pubmed.ncbi.nlm.nih.gov/9240913
https://pubmed.ncbi.nlm.nih.gov/9240913
Publikováno v:
The Journal of maternal-fetal medicine. 6(3)
The purpose of this study was to evaluate the prenatal characteristics of congenital nephrosis of the Finnish type (CNF). Patients presenting with elevated maternal serum and/or amniotic fluid alpha-fetoprotein levels, normal ultrasound examinations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3b46252d00608a85cd3e2c449b8885c5
https://pubmed.ncbi.nlm.nih.gov/9172059
https://pubmed.ncbi.nlm.nih.gov/9172059
Publikováno v:
Obstetrics and gynecology. 84(6)
To evaluate quantitative hCG measurements and transvaginal ultrasound in the diagnosis of ectopic pregnancy in patients presenting to the emergency department.A discriminatory zone for detecting the presence or absence of an intrauterine pregnancy by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c7a9e3b18270da227d9ae52576c1f455
https://pubmed.ncbi.nlm.nih.gov/7970455
https://pubmed.ncbi.nlm.nih.gov/7970455
Autor:
N C, Rose, M T, Mennuti
Publikováno v:
The Western journal of medicine. 159(3)
Second-trimester maternal serum screening is a noninvasive means of identifying pregnant women at an increased risk for various conditions including a fetus with open spina bifida, fetal Down syndrome, trisomy 18, multiple gestation, and adverse preg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::78b6b592b9b3fc4ddab9d1b35b5b3402
https://pubmed.ncbi.nlm.nih.gov/7694429
https://pubmed.ncbi.nlm.nih.gov/7694429
Publikováno v:
Clinical orthopaedics and related research. (293)
Osteogenesis imperfecta (OI) Type II is a rare heritable disorder of bone matrix that results in catastrophic congenital skeletal dysplasia. Two cases of OI Type II had symmetric rhizomelic skeletal dysplasia apparent on ultrasound at 16 and 20 weeks
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::47ed53fd98f4f72a0d894a38201da391
https://pubmed.ncbi.nlm.nih.gov/8339500
https://pubmed.ncbi.nlm.nih.gov/8339500
Publikováno v:
Obstetrics and gynecology. 75(6)
During an 8-year period, we managed 42 women with 101 pregnancies with previously diagnosed but uncorrected uterine malformations referred to our institution for high-risk obstetric care. All patients were managed under the same standardized protocol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ac3711f6c3a396a6ee72abfa9524ceff
https://pubmed.ncbi.nlm.nih.gov/2234730
https://pubmed.ncbi.nlm.nih.gov/2234730
Publikováno v:
The Journal of Bone & Joint Surgery. 71:1119-1129
Proximal femoral focal deficiency is a rare congenital malformation, characterized by a failure of normal development of the proximal part of the femur. To our knowledge, there have been no reports on the histology of fetal growth plates that are aff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e222b77f5258c2c87c421f446ca8992e
https://doi.org/10.2106/00004623-198971080-00001
https://doi.org/10.2106/00004623-198971080-00001
Publikováno v:
The Journal of bone and joint surgery. American volume. 71(8)
Proximal femoral focal deficiency is a rare congenital malformation, characterized by a failure of normal development of the proximal part of the femur. To our knowledge, there have been no reports on the histology of fetal growth plates that are aff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::58ce6f40b5276038f371bb37344bd151
https://pubmed.ncbi.nlm.nih.gov/2777837
https://pubmed.ncbi.nlm.nih.gov/2777837