-
1
-
-
1942442823
-
Neural tube defects and the spine
-
JP McGahan G Pilu DA Nyberg Neural tube defects and the spine DA Nyberg JP McGahan DH Pretorius G Pilu Diagnostic Imaging of Fetal Anomalies 2003 Lippincott Williams & Wilkins Philadelphia 291 334
-
(2003)
, pp. 291-334
-
-
McGahan, JP1
Pilu, G2
Nyberg, DA3
-
2
-
-
0018409294
-
Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macrencephaly and severe mental retardation: a new syndrome?
-
A Schinzel Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macrencephaly and severe mental retardation: a new syndrome? Helv Paediatr Acta 34 1979 141 146
-
(1979)
Helv Paediatr Acta
, vol.34
, pp. 141-146
-
-
Schinzel, A1
-
3
-
-
0036850976
-
De novo GLI3 mutation in acrocallosal syndrome: broadening the phenotypic spectrum of GLI3 defects and overlap with murine models
-
E Elson R Perveen D Donnai S Wall GCM Black De novo GLI3 mutation in acrocallosal syndrome: broadening the phenotypic spectrum of GLI3 defects and overlap with murine models J Med Genet 39 2002 804 806
-
(2002)
J Med Genet
, vol.39
, pp. 804-806
-
-
Elson, E1
Perveen, R2
Donnai, D3
Wall, S4
Black, GCM5
-
4
-
-
0026534950
-
Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2–p13.3
-
RA Pfeiffer G Legat U Trautmann Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2–p13.3 Ann Genet 35 1992 41 46
-
(1992)
Ann Genet
, vol.35
, pp. 41-46
-
-
Pfeiffer, RA1
Legat, G2
Trautmann, U3
-
5
-
-
85120138074
-
Acrocallosal syndrome
-
KL Jones Acrocallosal syndrome KL Jones Smith's Recognizable Patterns of Human Malformation 2006 Elsevier Saunders Philadelphia 252 253
-
(2006)
, pp. 252-253
-
-
Jones, KL1
-
7
-
-
0026516427
-
A family with one child with acrocallosal syndrome, one child with anencephaly-polydactyly, and parental consanguinity
-
S Cataltepe E Tuncbilek A family with one child with acrocallosal syndrome, one child with anencephaly-polydactyly, and parental consanguinity Eur J Pediatr 151 1992 288 290
-
(1992)
Eur J Pediatr
, vol.151
, pp. 288-290
-
-
Cataltepe, S1
Tuncbilek, E2
-
8
-
-
0028273979
-
The acrocallosal syndrome: expansion of the phenotypic spectrum
-
IW Lurie IV Naumchik EA Wulfsberg The acrocallosal syndrome: expansion of the phenotypic spectrum Clin Dysmorphol 3 1994 31 34
-
(1994)
Clin Dysmorphol
, vol.3
, pp. 31-34
-
-
Lurie, IW1
Naumchik, IV2
Wulfsberg, EA3
-
9
-
-
0030599893
-
Recurrent anencephaly as a primary manifestation of the acrocallosal syndrome
-
I Kedar A Amiel M Fejgin A Drugan Recurrent anencephaly as a primary manifestation of the acrocallosal syndrome Am J Med Genet 62 1996 415 416
-
(1996)
Am J Med Genet
, vol.62
, pp. 415-416
-
-
Kedar, I1
Amiel, A2
Fejgin, M3
Drugan, A4
-
10
-
-
0034063023
-
Sibs with anencephaly, anophthalmia, clefts, omphalocele, and polydactyly: hydrolethalus or acrocallosal syndrome?
-
B Christensen HG Blaas CV Isaksen B Roald KH Ørstavik Sibs with anencephaly, anophthalmia, clefts, omphalocele, and polydactyly: hydrolethalus or acrocallosal syndrome? Am J Med Genet 91 2000 231 234
-
(2000)
Am J Med Genet
, vol.91
, pp. 231-234
-
-
Christensen, B1
Blaas, HG2
Isaksen, CV3
Roald, B4
Ørstavik, KH5
-
12
-
-
0034723736
-
Radioulnar synostosis, radial ray abnormalities, and severe malformations in the male: a new X-linked dominant multiple congenital anomalies syndrome?
-
S Manouvrier A Moerman A Coeslier L Devisme O Boute M Le Merrer Radioulnar synostosis, radial ray abnormalities, and severe malformations in the male: a new X-linked dominant multiple congenital anomalies syndrome? Am J Med Genet 90 2000 351 355
-
(2000)
Am J Med Genet
, vol.90
, pp. 351-355
-
-
Manouvrier, S1
Moerman, A2
Coeslier, A3
Devisme, L4
Boute, O5
Le Merrer, M6
-
13
-
-
0002033793
-
Skeletal dysplasia
-
th edition 1996 Mosby St Louis 745 951
-
(1996)
, pp. 745-951
-
-
Lachman, RS1
-
14
-
-
0027422076
-
Lethal short rib-polydactyly syndromes: further evidence for their overlapping in a continuous spectrum
-
M-L Martínez-Frías E Bermejo M Urioste H Huertas I Arroyo Lethal short rib-polydactyly syndromes: further evidence for their overlapping in a continuous spectrum J Med Genet 30 1993 937 941
-
(1993)
J Med Genet
, vol.30
, pp. 937-941
-
-
Martínez-Frías, M-L1
Bermejo, E2
Urioste, M3
Huertas, H4
Arroyo, I5
-
15
-
-
0032845494
-
Short ribpolydactyly syndrome: more evidence of a continuous spectrum
-
K Sarafoglou EF Funai N Fefferman Short ribpolydactyly syndrome: more evidence of a continuous spectrum Clin Genet 56 1999 145 148
-
(1999)
Clin Genet
, vol.56
, pp. 145-148
-
-
Sarafoglou, K1
Funai, EF2
Fefferman, N3
-
16
-
-
0033961102
-
Jeune asphyxiating thoracic dystrophy and short-rib polydactyly type III (Verma-Naumoff) are variants of the same disorder
-
NC Ho CA Francomano M van Allen Jeune asphyxiating thoracic dystrophy and short-rib polydactyly type III (Verma-Naumoff) are variants of the same disorder Am J Med Genet 90 2000 310 314
-
(2000)
Am J Med Genet
, vol.90
, pp. 310-314
-
-
Ho, NC1
Francomano, CA2
van Allen, M3
-
17
-
-
0036707795
-
Diagnostic dilemmas in the short rib-polydactyly syndrome group
-
NH Elçioglu CM Hall Diagnostic dilemmas in the short rib-polydactyly syndrome group Am J Med Genet 111 2002 392 400
-
(2002)
Am J Med Genet
, vol.111
, pp. 392-400
-
-
Elçioglu, NH1
Hall, CM2
-
18
-
-
0027454440
-
Short rib-polydactyly syndrome (SRPS) with anencephaly and other central nervous system anomalies: a new type of SRPS or a more severe expression of a known SRPS entity?
-
ML Martínez-Frías E Bermejo M Urioste J Egüés JA López Soler Short rib-polydactyly syndrome (SRPS) with anencephaly and other central nervous system anomalies: a new type of SRPS or a more severe expression of a known SRPS entity? Am J Med Genet 47 1993 782 787
-
(1993)
Am J Med Genet
, vol.47
, pp. 782-787
-
-
Martínez-Frías, ML1
Bermejo, E2
Urioste, M3
Egüés, J4
López Soler, JA5
-
19
-
-
0030734258
-
Disorganization in mice and humans and its relation to sporadic birth defects
-
NH Robin N Abbadi SE McCandless JH Nadeau Disorganization in mice and humans and its relation to sporadic birth defects Am J Med Genet 73 1997 425 436
-
(1997)
Am J Med Genet
, vol.73
, pp. 425-436
-
-
Robin, NH1
Abbadi, N2
McCandless, SE3
Nadeau, JH4
-
20
-
-
0036155964
-
Intestinal mucosa on top of a rudimentary occipital meningocele in amniotic rupture sequence: disorganization-like syndrome, homeotic transformation, abnormal surface encounter or endoectodermal adhesion?
-
HJ ten Donkelaar BC Hamel E Hartman JA van Lier P Wesseling Intestinal mucosa on top of a rudimentary occipital meningocele in amniotic rupture sequence: disorganization-like syndrome, homeotic transformation, abnormal surface encounter or endoectodermal adhesion? Clin Dysmorphol 11 2002 9 13
-
(2002)
Clin Dysmorphol
, vol.11
, pp. 9-13
-
-
ten Donkelaar, HJ1
Hamel, BC2
Hartman, E3
van Lier, JA4
Wesseling, P5
-
22
-
-
0021183437
-
The hemi 3 syndrome. Hemihypertrophy, hemihypaesthesia, hemiareflexia and scoliosis
-
K Nudleman E Andermann F Andermann G Bertrand E Rogala The hemi 3 syndrome. Hemihypertrophy, hemihypaesthesia, hemiareflexia and scoliosis Brain 107 1984 533 546
-
(1984)
Brain
, vol.107
, pp. 533-546
-
-
Nudleman, K1
Andermann, E2
Andermann, F3
Bertrand, G4
Rogala, E5
-
23
-
-
0018937171
-
Possible X-linked anencephaly and spina bifida: report of a kindred
-
HV Toriello ST Warren JA Lindstrom Possible X-linked anencephaly and spina bifida: report of a kindred Am J Med Genet 6 1980 119 121
-
(1980)
Am J Med Genet
, vol.6
, pp. 119-121
-
-
Toriello, HV1
Warren, ST2
Lindstrom, JA3
-
24
-
-
0021333265
-
Neural tube defects as an X-linked condition
-
M Baraitser J Burn Neural tube defects as an X-linked condition Am J Med Genet 17 1984 383 385
-
(1984)
Am J Med Genet
, vol.17
, pp. 383-385
-
-
Baraitser, M1
Burn, J2
-
25
-
-
0021504552
-
Report of a third kindred with X-linked anencephaly/spina bifida
-
HV Toriello Report of a third kindred with X-linked anencephaly/spina bifida Am J Med Genet 19 1984 411 412
-
(1984)
Am J Med Genet
, vol.19
, pp. 411-412
-
-
Toriello, HV1
-
27
-
-
0028298578
-
Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects
-
R Newton P Stanier S Loughna Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects Clin Genet 45 1994 241 249
-
(1994)
Clin Genet
, vol.45
, pp. 241-249
-
-
Newton, R1
Stanier, P2
Loughna, S3
-
30
-
-
0029688862
-
Lumbosacral spina bifida and myeloschizis in a female foetus with de novo X/autosomal translocation (t(X;22)(q27;q121))
-
JP Fryns K Devriendt P Moerman Lumbosacral spina bifida and myeloschizis in a female foetus with de novo X/autosomal translocation (t(X;22)(q27;q121)) Genet Couns 7 1996 159 160
-
(1996)
Genet Couns
, vol.7
, pp. 159-160
-
-
Fryns, JP1
Devriendt, K2
Moerman, P3
-
31
-
-
0034667325
-
Identification and characterization of an Xq26–q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genes
-
FA Hol MT Schepens SE van Beersum Identification and characterization of an Xq26–q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genes Genomics 69 2000 174 181
-
(2000)
Genomics
, vol.69
, pp. 174-181
-
-
Hol, FA1
Schepens, MT2
van Beersum, SE3
-
34
-
-
0029839899
-
Human Cart-1: structural organization, chromosomal localization, and functional analysis of a cartilage-specific homeodomain cDNA
-
DF Gordon J Wagner BL Atkinson M Chiono R Berry J Sikela A Gutierrez-Hartmann Human Cart-1: structural organization, chromosomal localization, and functional analysis of a cartilage-specific homeodomain cDNA DNA Cell Biol 15 1996 531 541
-
(1996)
DNA Cell Biol
, vol.15
, pp. 531-541
-
-
Gordon, DF1
Wagner, J2
Atkinson, BL3
Chiono, M4
Berry, R5
Sikela, J6
Gutierrez-Hartmann, A7
-
35
-
-
0029946542
-
Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene
-
Q Zhao RR Behringer B de Crombrugghe Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene Nat Genet 13 1996 275 283
-
(1996)
Nat Genet
, vol.13
, pp. 275-283
-
-
Zhao, Q1
Behringer, RR2
de Crombrugghe, B3
-
36
-
-
0019389699
-
Schisis-association
-
A Czeizel Schisis-association Am J Med Genet 10 1981 25 35
-
(1981)
Am J Med Genet
, vol.10
, pp. 25-35
-
-
Czeizel, A1
-
37
-
-
0030997095
-
Epidemiological analysis of the schisis association in the Spanish registry of congenital malformations
-
ML Martínez-Frías JL Frías E Bermejo E Rodríguez-Pinilla M Urioste Epidemiological analysis of the schisis association in the Spanish registry of congenital malformations Am J Med Genet 70 1997 16 23
-
(1997)
Am J Med Genet
, vol.70
, pp. 16-23
-
-
Martínez-Frías, ML1
Frías, JL2
Bermejo, E3
Rodríguez-Pinilla, E4
Urioste, M5
-
38
-
-
0017209303
-
Craniofacial duplication (diprosopus) in a twin
-
DG Changaris MH McGavran Craniofacial duplication (diprosopus) in a twin Arch Pathol Lab Med 100 1976 392 394
-
(1976)
Arch Pathol Lab Med
, vol.100
, pp. 392-394
-
-
Changaris, DG1
McGavran, MH2
-
39
-
-
0017688879
-
Anencephaly with incomplete twinning (diprosopus)
-
VM Riccardi CA Bergmann Anencephaly with incomplete twinning (diprosopus) Teratology 16 1977 137 140
-
(1977)
Teratology
, vol.16
, pp. 137-140
-
-
Riccardi, VM1
Bergmann, CA2
-
40
-
-
0020054048
-
Facial duplication: case, review, and embryogenesis
-
M Barr Jr Facial duplication: case, review, and embryogenesis Teratology 25 1982 153 159
-
(1982)
Teratology
, vol.25
, pp. 153-159
-
-
Barr, M1
-
42
-
-
0021914654
-
Obstetric significance of fetal craniofacial duplication. A case report
-
FA Chervenak MM Pinto CI Heller H Norooz Obstetric significance of fetal craniofacial duplication. A case report J Reprod Med 30 1985 74 76
-
(1985)
J Reprod Med
, vol.30
, pp. 74-76
-
-
Chervenak, FA1
Pinto, MM2
Heller, CI3
Norooz, H4
-
47
-
-
0027496619
-
Diprosopus: a pregastrulation defect involving the head, neural tube, heart, and diaphragm
-
R Sharony SH Pepkowitz H Hixon GA Machin JM Graham Jr Diprosopus: a pregastrulation defect involving the head, neural tube, heart, and diaphragm Birth Defects Orig Artic Ser 29 1993 201 209
-
(1993)
Birth Defects Orig Artic Ser
, vol.29
, pp. 201-209
-
-
Sharony, R1
Pepkowitz, SH2
Hixon, H3
Machin, GA4
Graham, JM5
-
48
-
-
0345491034
-
Diprosopus (partially duplicated head) associated with anencephaly: a case report
-
A al Muti Zaitoun J Chang M Booker Diprosopus (partially duplicated head) associated with anencephaly: a case report Pathol Res Pract 195 1999 45 50
-
(1999)
Pathol Res Pract
, vol.195
, pp. 45-50
-
-
al Muti Zaitoun, A1
Chang, J2
Booker, M3
-
49
-
-
1842736344
-
Diprosopus associated with neural tube defect and facial cleft in the first trimester
-
Y Bulbul CL Drummond Y Hillion L Bidat Y Ville Diprosopus associated with neural tube defect and facial cleft in the first trimester Fetal Diagn Ther 19 2004 246 250
-
(2004)
Fetal Diagn Ther
, vol.19
, pp. 246-250
-
-
Bulbul, Y1
Drummond, CL2
Hillion, Y3
Bidat, L4
Ville, Y5
-
50
-
-
20044375992
-
An anencephalic monocephalus diprosopus “headed twin”: postmortem and CT findings with emphasis on the cranial bones
-
G Ekinci S Balci C Erzen An anencephalic monocephalus diprosopus “headed twin”: postmortem and CT findings with emphasis on the cranial bones Turk J Pediatr 47 2005 195 198
-
(2005)
Turk J Pediatr
, vol.47
, pp. 195-198
-
-
Ekinci, G1
Balci, S2
Erzen, C3
-
52
-
-
0023620111
-
Fetal valproate syndrome: is there a recognisable phenotype?
-
RM Winter D Donnai J Burn SM Tucker Fetal valproate syndrome: is there a recognisable phenotype? J Med Genet 24 1987 692 695
-
(1987)
J Med Genet
, vol.24
, pp. 692-695
-
-
Winter, RM1
Donnai, D2
Burn, J3
Tucker, SM4
-
53
-
-
0023863338
-
Verification of the fetal valproate syndrome phenotype
-
HH Ardinger JF Atkin RD Blackston Verification of the fetal valproate syndrome phenotype Am J Med Genet 29 1988 171 185
-
(1988)
Am J Med Genet
, vol.29
, pp. 171-185
-
-
Ardinger, HH1
Atkin, JF2
Blackston, RD3
-
56
-
-
0022571613
-
In-utero exposure to valproate and neural tube defects
-
D Lindhout D Schmidt In-utero exposure to valproate and neural tube defects Lancet 1 1986 1392 1393
-
(1986)
Lancet
, vol.1
, pp. 1392-1393
-
-
Lindhout, D1
Schmidt, D2
-
62
-
-
0021176145
-
Sacral meningocele with conotruncal heart defects: a possible autosomal recessive trait
-
BG Kousseff Sacral meningocele with conotruncal heart defects: a possible autosomal recessive trait Pediatrics 74 1984 395 398
-
(1984)
Pediatrics
, vol.74
, pp. 395-398
-
-
Kousseff, BG1
-
64
-
-
0027407062
-
Waardenburg syndrome and myelomeningocele in a family
-
S Chatkupt S Chatkupt WG Johnson Waardenburg syndrome and myelomeningocele in a family J Med Genet 30 1993 83 84
-
(1993)
J Med Genet
, vol.30
, pp. 83-84
-
-
Chatkupt, S1
Chatkupt, S2
Johnson, WG3
-
65
-
-
0032477782
-
Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: possible digenic inheritance of a neural tube defect
-
JS Nye N Balkin H Lucas PA Knepper DG McLone J Charrow Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: possible digenic inheritance of a neural tube defect Am J Med Genet 75 1998 401 408
-
(1998)
Am J Med Genet
, vol.75
, pp. 401-408
-
-
Nye, JS1
Balkin, N2
Lucas, H3
Knepper, PA4
McLone, DG5
Charrow, J6
-
66
-
-
0028954840
-
A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome
-
FA Hol BC Hamel MP Geurds RA Mullaart FG Barr RA Macina EC Mariman A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome J Med Genet 32 1995 52 56
-
(1995)
J Med Genet
, vol.32
, pp. 52-56
-
-
Hol, FA1
Hamel, BC2
Geurds, MP3
Mullaart, RA4
Barr, FG5
Macina, RA6
Mariman, EC7
-
67
-
-
3242704306
-
Molecular cytogenetic characterization of multiple intrachromosomal rearrangements of chromosome 2q in a patient with Waardenburg's syndrome and other congenital defects
-
SH Shim HE Wyandt DM McDonald-McGinn EZ Zackai A Milunsky Molecular cytogenetic characterization of multiple intrachromosomal rearrangements of chromosome 2q in a patient with Waardenburg's syndrome and other congenital defects Clin Genet 66 2004 46 52
-
(2004)
Clin Genet
, vol.66
, pp. 46-52
-
-
Shim, SH1
Wyandt, HE2
McDonald-McGinn, DM3
Zackai, EZ4
Milunsky, A5
-
68
-
-
33847052754
-
Prenatal diagnosis and genetic counseling in a case of spina bifida in a family with Waardenburg syndrome type I
-
A Kujat VP Veith R Faber UG Froster Prenatal diagnosis and genetic counseling in a case of spina bifida in a family with Waardenburg syndrome type I Fetal Diagn Ther 22 2007 155 158
-
(2007)
Fetal Diagn Ther
, vol.22
, pp. 155-158
-
-
Kujat, A1
Veith, VP2
Faber, R3
Froster, UG4
-
70
-
-
0029638071
-
Possible homozygous Waardenburg syndrome in a fetus with exencephaly
-
S Aymé N Philip Possible homozygous Waardenburg syndrome in a fetus with exencephaly Am J Med Genet 59 1995 263 265
-
(1995)
Am J Med Genet
, vol.59
, pp. 263-265
-
-
Aymé, S1
Philip, N2
-
71
-
-
0035873403
-
Neural tube defects in relation to use of folic acid antagonists during pregnancy
-
S Hernández-Díaz MM Werler AM Walker AA Mitchell Neural tube defects in relation to use of folic acid antagonists during pregnancy Am J Epidemiol 153 2001 961 968
-
(2001)
Am J Epidemiol
, vol.153
, pp. 961-968
-
-
Hernández-Díaz, S1
Werler, MM2
Walker, AM3
Mitchell, AA4
-
72
-
-
0026845320
-
The risk of spina bifida aperta after first-trimester exposure to valproate in a prenatal cohort
-
JG Omtzigt FJ Los DE Grobbee The risk of spina bifida aperta after first-trimester exposure to valproate in a prenatal cohort Neurology 42 4 Suppl 5 1992 119 125
-
(1992)
Neurology
, vol.42
, Issue.4 Suppl 5
, pp. 119-125
-
-
Omtzigt, JG1
Los, FJ2
Grobbee, DE3
-
73
-
-
0026030573
-
Spina bifida in infants of women treated with carbamazepine during pregnancy
-
FW Rosa Spina bifida in infants of women treated with carbamazepine during pregnancy N Engl J Med 324 1991 674 677
-
(1991)
N Engl J Med
, vol.324
, pp. 674-677
-
-
Rosa, FW1
-
74
-
-
0028426919
-
Maternal carbamazepine and infant spina bifida
-
AJ Källén Maternal carbamazepine and infant spina bifida Reprod Toxicol 8 1994 203 205
-
(1994)
Reprod Toxicol
, vol.8
, pp. 203-205
-
-
Källén, AJ1
-
75
-
-
0036010428
-
The teratogenic effect of carbamazepine: a meta-analysis of 1255 exposures
-
S Matalon S Schechtman G Goldzweig A Ornoy The teratogenic effect of carbamazepine: a meta-analysis of 1255 exposures Reprod Toxicol 16 2002 9 17
-
(2002)
Reprod Toxicol
, vol.16
, pp. 9-17
-
-
Matalon, S1
Schechtman, S2
Goldzweig, G3
Ornoy, A4
-
76
-
-
27144476821
-
Maternal diabetes and neural tube defects: prenatal diagnosis of lumbosacral myelomeningocele, ventriculomegaly, Arnold-Chiari malformation and foot deformities in a pregnancy with poor maternal metabolic control, and review of the literature
-
CP Chen Maternal diabetes and neural tube defects: prenatal diagnosis of lumbosacral myelomeningocele, ventriculomegaly, Arnold-Chiari malformation and foot deformities in a pregnancy with poor maternal metabolic control, and review of the literature Genet Couns 16 2005 313 316
-
(2005)
Genet Couns
, vol.16
, pp. 313-316
-
-
Chen, CP1
-
77
-
-
0018363182
-
Malformations in infants of diabetic mothers occur before the seventh gestational week: implications for treatment
-
JL Mills L Baker AS Goldman Malformations in infants of diabetic mothers occur before the seventh gestational week: implications for treatment Diabetes 28 1979 292 293
-
(1979)
Diabetes
, vol.28
, pp. 292-293
-
-
Mills, JL1
Baker, L2
Goldman, AS3
-
78
-
-
5444267372
-
Risk of congenital anomalies detected during antenatal serum screening in women with pregestational diabetes
-
JG Ray MJ Vermeulen C Meier PR Wyatt Risk of congenital anomalies detected during antenatal serum screening in women with pregestational diabetes QJM 97 2004 651 653
-
(2004)
QJM
, vol.97
, pp. 651-653
-
-
Ray, JG1
Vermeulen, MJ2
Meier, C3
Wyatt, PR4
-
79
-
-
0032858266
-
Genotoxicity and diabetic embryopathy: impaired expression of developmental control genes as a cause of defective morphogenesis
-
TI Chang MR Loeken Genotoxicity and diabetic embryopathy: impaired expression of developmental control genes as a cause of defective morphogenesis Semin Reprod Endocrinol 17 1999 153 165
-
(1999)
Semin Reprod Endocrinol
, vol.17
, pp. 153-165
-
-
Chang, TI1
Loeken, MR2
-
80
-
-
0030994305
-
Neural tube defects in embryos of diabetic mice: role of the Pax-3 gene and apoptosis
-
SA Phelan M Ito MR Loeken Neural tube defects in embryos of diabetic mice: role of the Pax-3 gene and apoptosis Diabetes 46 1997 1189 1197
-
(1997)
Diabetes
, vol.46
, pp. 1189-1197
-
-
Phelan, SA1
Ito, M2
Loeken, MR3
-
81
-
-
0033513480
-
Evidence that elevated glucose causes altered gene expression, apoptosis, and neural tube defects in a mouse model of diabetic pregnancy
-
EL Fine M Horal TI Chang G Fortin MR Loeken Evidence that elevated glucose causes altered gene expression, apoptosis, and neural tube defects in a mouse model of diabetic pregnancy Diabetes 48 1999 2454 2462
-
(1999)
Diabetes
, vol.48
, pp. 2454-2462
-
-
Fine, EL1
Horal, M2
Chang, TI3
Fortin, G4
Loeken, MR5
-
82
-
-
0037955858
-
Oxidant regulation of gene expression and neural tube development: insights gained from diabetic pregnancy on molecular causes of neural tube defects
-
TI Chang M Horal SK Jain F Wang R Patel MR Loeken Oxidant regulation of gene expression and neural tube development: insights gained from diabetic pregnancy on molecular causes of neural tube defects Diabetologia 46 2003 538 545
-
(2003)
Diabetologia
, vol.46
, pp. 538-545
-
-
Chang, TI1
Horal, M2
Jain, SK3
Wang, F4
Patel, R5
Loeken, MR6
-
83
-
-
0036723777
-
Polymorphic susceptibility to the molecular causes of neural tube defects during diabetic embryopathy
-
L Pani M Horal MR Loeken Polymorphic susceptibility to the molecular causes of neural tube defects during diabetic embryopathy Diabetes 51 2002 2871 2874
-
(2002)
Diabetes
, vol.51
, pp. 2871-2874
-
-
Pani, L1
Horal, M2
Loeken, MR3
-
84
-
-
0037087629
-
Rescue of neural tube defects in Pax-3-deficient embryos by p53 loss of function: implications for Pax-3-dependent development and tumorigenesis
-
L Pani M Horal MR Loeken Rescue of neural tube defects in Pax-3-deficient embryos by p53 loss of function: implications for Pax-3-dependent development and tumorigenesis Genes Dev 16 2002 676 680
-
(2002)
Genes Dev
, vol.16
, pp. 676-680
-
-
Pani, L1
Horal, M2
Loeken, MR3
-
85
-
-
2542446440
-
Free radicals and birth defects
-
MR Loeken Free radicals and birth defects J Matern Fetal Neonatal Med 15 2004 6 14
-
(2004)
J Matern Fetal Neonatal Med
, vol.15
, pp. 6-14
-
-
Loeken, MR1
-
86
-
-
17844386819
-
Current perspectives on the causes of neural tube defects resulting from diabetic pregnancy
-
MR Loeken Current perspectives on the causes of neural tube defects resulting from diabetic pregnancy Am J Med Genet C Semin Med Genet 135 2005 77 87
-
(2005)
Am J Med Genet C Semin Med Genet
, vol.135
, pp. 77-87
-
-
Loeken, MR1
-
89
-
-
0029869817
-
Risk of neural tube defectaffected pregnancies among obese women
-
GM Shaw EM Velie D Schaffer Risk of neural tube defectaffected pregnancies among obese women JAMA 275 1996 1093 1096
-
(1996)
JAMA
, vol.275
, pp. 1093-1096
-
-
Shaw, GM1
Velie, EM2
Schaffer, D3
-
90
-
-
0033871680
-
Maternal height and prepregnancy body mass index as risk factors for selected congenital anomalies
-
GM Shaw K Todoroff DM Schaffer S Selvin Maternal height and prepregnancy body mass index as risk factors for selected congenital anomalies Paediatr Perinat Epidemiol 14 2000 234 239
-
(2000)
Paediatr Perinat Epidemiol
, vol.14
, pp. 234-239
-
-
Shaw, GM1
Todoroff, K2
Schaffer, DM3
Selvin, S4
-
91
-
-
0642310644
-
Neural tube defects associated with maternal periconceptional dietary intake of simple sugars and glycemic index
-
GM Shaw T Quach V Nelson SL Carmichael DM Schaffer S Selvin W Yang Neural tube defects associated with maternal periconceptional dietary intake of simple sugars and glycemic index Am J Clin Nutr 78 2003 972 978
-
(2003)
Am J Clin Nutr
, vol.78
, pp. 972-978
-
-
Shaw, GM1
Quach, T2
Nelson, V3
Carmichael, SL4
Schaffer, DM5
Selvin, S6
Yang, W7
-
92
-
-
0029869816
-
Prepregnant weight in relation to risk of neural tube defects
-
MM Werler C Louik S Shapiro AA Mitchell Prepregnant weight in relation to risk of neural tube defects JAMA 275 1996 1089 1092
-
(1996)
JAMA
, vol.275
, pp. 1089-1092
-
-
Werler, MM1
Louik, C2
Shapiro, S3
Mitchell, AA4
-
93
-
-
0029799199
-
Is maternal obesity a risk factor for anencephaly and spina bifida?
-
ML Watkins KS Scanlon J Mulinare MJ Khoury Is maternal obesity a risk factor for anencephaly and spina bifida? Epidemiology 7 1996 507 512
-
(1996)
Epidemiology
, vol.7
, pp. 507-512
-
-
Watkins, ML1
Scanlon, KS2
Mulinare, J3
Khoury, MJ4
-
95
-
-
0035214757
-
Effects of hyperinsulinemia and obesity on risk of neural tube defects among Mexican Americans
-
KA Hendricks OM Nuno L Suarez R Larsen Effects of hyperinsulinemia and obesity on risk of neural tube defects among Mexican Americans Epidemiology 12 2001 630 635
-
(2001)
Epidemiology
, vol.12
, pp. 630-635
-
-
Hendricks, KA1
Nuno, OM2
Suarez, L3
Larsen, R4
-
96
-
-
13744253123
-
Maternal obesity, gestational diabetes, and central nervous system birth defects
-
JL Anderson DK Waller MA Canfield GM Shaw ML Watkins MM Werler Maternal obesity, gestational diabetes, and central nervous system birth defects Epidemiology 16 2005 87 92
-
(2005)
Epidemiology
, vol.16
, pp. 87-92
-
-
Anderson, JL1
Waller, DK2
Canfield, MA3
Shaw, GM4
Watkins, ML5
Werler, MM6
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