115 related articles for article (PubMed ID: 29980223)
21. Cyclopia and proboscis - the extreme end of holoprosencephaly.
Măluţan AM; Dudea M; Ciortea R; Mureşan M; Bucuri CE; Mihu C; Mihu D
Rom J Morphol Embryol; 2017; 58(4):1555-1559. PubMed ID: 29556657
[TBL] [Abstract][Full Text] [Related]
22. Early-onset preeclampsia appears to discourage subsequent pregnancy but the risks may be overestimated.
Seeho SK; Algert CS; Roberts CL; Ford JB
Am J Obstet Gynecol; 2016 Dec; 215(6):785.e1-785.e8. PubMed ID: 27457117
[TBL] [Abstract][Full Text] [Related]
23. Association Between Fetal Congenital Heart Defects and Maternal Risk of Hypertensive Disorders of Pregnancy in the Same Pregnancy and Across Pregnancies.
Boyd HA; Basit S; Behrens I; Leirgul E; Bundgaard H; Wohlfahrt J; Melbye M; Øyen N
Circulation; 2017 Jul; 136(1):39-48. PubMed ID: 28424221
[TBL] [Abstract][Full Text] [Related]
24. Semilobar Holoprosencephaly Caused by a Novel and De Novo
Nonkulovski D; Sofijanova A; Spasovska T; Gorjan M; Muaremoska-Kanzoska L; Arsov T
Balkan J Med Genet; 2023 May; 25(2):71-76. PubMed ID: 37265970
[TBL] [Abstract][Full Text] [Related]
25. Proteinuria: A presenting manifestation of mirror syndrome in pregnancy
.
Banoth P; Chaudhary K
Clin Nephrol; 2018 Jul; 90(1):60-63. PubMed ID: 29633703
[TBL] [Abstract][Full Text] [Related]
26. Antenatal sonographic diagnosis of semilobar holoprosencephaly with associated cleft lip and palate.
Naikwadi A; Rege R; Hameed S
BJR Case Rep; 2019 Feb; 5(1):20180013. PubMed ID: 31131114
[TBL] [Abstract][Full Text] [Related]
27. Semilobar Holoprosencephaly: Capacious Anomaly in the Cephalad.
Veluchamy M; Murugan M
Cureus; 2020 Jul; 12(7):e9181. PubMed ID: 32802616
[TBL] [Abstract][Full Text] [Related]
28. Nationwide epidemiological survey of holoprosencephaly in Japan.
Abe Y; Araki R; Sobajima H; Tamura M; Kunikata T; Ohtake A; Yamanouchi H
Pediatr Int; 2020 May; 62(5):593-599. PubMed ID: 31886593
[TBL] [Abstract][Full Text] [Related]
29. Holoprosencephaly in Patau Syndrome.
Schlosser AS; Costa GJC; Silva HSD; Mello JLM; Gomes LO; Onoyama MMO; Costa TMC
Rev Paul Pediatr; 2023; 41():e2022027. PubMed ID: 36921175
[TBL] [Abstract][Full Text] [Related]
30. Atypical preeclampsia-eclampsia syndrome at 18 weeks of gestation: A case report.
Aja-Okorie U; Ngene NC
Case Rep Womens Health; 2022 Oct; 36():e00470. PubMed ID: 36467289
[TBL] [Abstract][Full Text] [Related]
31. Alobar holoprosencephaly in mining-related areas of the Eastern region of the Democratic Republic of the Congo: A case series.
Mudekereza PS; Mudekereza JB; Bahizire GM; Lekuya HM; Mudekereza EA; Zabadayi GM; Budema PM; Balungwe PB; Chimanuka D; Mubenga LM
Birth Defects Res; 2021 Nov; 113(18):1333-1338. PubMed ID: 34519175
[TBL] [Abstract][Full Text] [Related]
32. Overlapping holoprosencephaly-polydactyl syndrome and asphyxiating thoracic dystrophy, an incidental finding in late prenatal ultrasound: A rare case report.
Sereke SG; Oriekot A; Bongomin F
Clin Case Rep; 2021 Mar; 9(3):1577-1582. PubMed ID: 33768892
[TBL] [Abstract][Full Text] [Related]
33. Fetal Magnetic Resonance Imaging (MRI) in Holoprosencephaly and Associations With Clinical Outcome: Implications for Fetal Counseling.
Riddle A; Nagaraj U; Hopkin RJ; Kline-Fath B; Venkatesan C
J Child Neurol; 2021 Apr; 36(5):357-364. PubMed ID: 33226281
[TBL] [Abstract][Full Text] [Related]
34. Atypical Presentation of Antenatal Eclampsia.
Maturu MVS; Pappu S; Datla AV; Devara A; Dalai S
Cureus; 2022 May; 14(5):e24745. PubMed ID: 35686275
[TBL] [Abstract][Full Text] [Related]
35. Semilobarholoprosencephaly - A Dreading Congenital Anomaly.
Lakhkar BB; Lakhkar BN; Lakhkar BB
J Clin Diagn Res; 2017 Jun; 11(6):TD03-TD04. PubMed ID: 28764265
[TBL] [Abstract][Full Text] [Related]
36. Preeclampsia: A Possible Complication of Primary Hyperparathyroidism.
Alharbi BA; Alqahtani MA; Hmoud M; Alhejaili EA; Badros R
Case Rep Obstet Gynecol; 2016; 2016():7501263. PubMed ID: 27340578
[TBL] [Abstract][Full Text] [Related]
37. Congenital hyporhinia with associated malformations: Case report of a rare congenital anomaly.
Mlay K; Chussi D; Mtenga P; Shija P; Msele A
Clin Case Rep; 2023 Mar; 11(3):e7099. PubMed ID: 36937628
[TBL] [Abstract][Full Text] [Related]
38. Fusion of lower limbs with severe urogenital malformation in a newborn, a rare congenital clinical syndrome: case report.
Al Hadhoud F; Kamal AH; Al Anjari A; Diejomaoh MF
Int Med Case Rep J; 2017; 10():313-317. PubMed ID: 29033614
[TBL] [Abstract][Full Text] [Related]
39. The diagnosis of the middle interhemispheric variant of holoprosencephaly with fetal MRI.
Garrido Márquez I; Fernández Navarro L; Moya Sánchez E
Radiologia (Engl Ed); 2022; 64(4):375-378. PubMed ID: 36030084
[TBL] [Abstract][Full Text] [Related]
40. Nongenetic risk factors for holoprosencephaly: An updated review of the epidemiologic literature.
Summers AD; Reefhuis J; Taliano J; Rasmussen SA
Am J Med Genet C Semin Med Genet; 2018 Jun; 178(2):151-164. PubMed ID: 29761639
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
