Schwartz M - Search Results

1

Naturally conceived twins with monochorionic placentation have the highest risk of fetal loss.

Sperling L, Kiil C, Larsen LU, Qvist I, Schwartz M, Jørgensen C, Skajaa K, Bang J, Tabor A. Sperling L, et al. Among authors: schwartz m. Ultrasound Obstet Gynecol. 2006 Oct;28(5):644-52. doi: 10.1002/uog.3820. Ultrasound Obstet Gynecol. 2006. PMID: 17001739 Free article.

2

Detection of chromosomal abnormalities, congenital abnormalities and transfusion syndrome in twins.

Sperling L, Kiil C, Larsen LU, Brocks V, Wojdemann KR, Qvist I, Schwartz M, Jørgensen C, Espersen G, Skajaa K, Bang J, Tabor A. Sperling L, et al. Among authors: schwartz m. Ultrasound Obstet Gynecol. 2007 May;29(5):517-26. doi: 10.1002/uog.3918. Ultrasound Obstet Gynecol. 2007. PMID: 17429797 Free article.

3

Dizygotic monochorionic twin pregnancy conceived following intracytoplasmic sperm injection treatment and complicated by twin-twin transfusion syndrome and blood chimerism.

Ekelund CK, Skibsted L, Søgaard K, Main KM, Dziegiel MH, Schwartz M, Moeller N, Roos L, Tabor A. Ekelund CK, et al. Among authors: schwartz m. Ultrasound Obstet Gynecol. 2008 Nov;32(6):832-4. doi: 10.1002/uog.6221. Ultrasound Obstet Gynecol. 2008. PMID: 18956441 Free article.

4

Early prenatal direct gene diagnosis of cystic fibrosis in a twin pregnancy and subsequent selective termination.

Jørgensen FS, Bang J, Tranebjaerg L, Berge LN, Eik-Nes SH, Schwartz M. Jørgensen FS, et al. Among authors: schwartz m. Prenat Diagn. 1994 Feb;14(2):149-52. doi: 10.1002/pd.1970140212. Prenat Diagn. 1994. PMID: 8183851

5

[Prenatal diagnosis of hemophilia].

Philip J, Bang J, Holmberg L, Berthelsen JG, Brandt NJ, Fernandes A, Schwartz M. Philip J, et al. Among authors: schwartz m. Ugeskr Laeger. 1979 Dec 3;141(49):3360-2. Ugeskr Laeger. 1979. PMID: 524515 Danish. No abstract available.

6

Prenatal diagnosis of chronic granulomatous disease.

Borregaard N, Bang J, Berthelsen JG, Johansen KS, Koch C, Philip J, Rasmussen K, Schwartz M, Therkelsen AJ, Valerius NH. Borregaard N, et al. Among authors: schwartz m. Lancet. 1982 Jan 9;1(8263):114. doi: 10.1016/s0140-6736(82)90258-6. Lancet. 1982. PMID: 6119486 No abstract available.

7

Erroneous genetic sex determination of a newborn twin girl due to chimerism caused by foetal blood transfusion. A case report.

Johannsen TH, Lundsteen C, Visfeldt J, Schwartz M, Petersen BL, Byskov AG, Müller J. Johannsen TH, et al. Among authors: schwartz m. Horm Res. 2003;60(3):148-51. doi: 10.1159/000072527. Horm Res. 2003. PMID: 12931043

8

Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophy.

Bisgaard AM, Kirchhoff M, Nielsen JE, Kibaek M, Lund A, Schwartz M, Christensen E. Bisgaard AM, et al. Among authors: schwartz m. Clin Genet. 2009 Feb;75(2):175-9. doi: 10.1111/j.1399-0004.2008.01113.x. Epub 2008 Nov 21. Clin Genet. 2009. PMID: 19054018

9

Computer-assisted prenatal aneuploidy screening for chromosome 13, 18, 21, X and Y based on multiplex ligation-dependent probe amplification (MLPA).

Gerdes T, Kirchhoff M, Lind AM, Larsen GV, Schwartz M, Lundsteen C. Gerdes T, et al. Among authors: schwartz m. Eur J Hum Genet. 2005 Feb;13(2):171-5. doi: 10.1038/sj.ejhg.5201307. Eur J Hum Genet. 2005. PMID: 15483643

10

Long-Term Gynecological Outcomes in Women with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency.

Johannsen TH, Ripa CP, Carlsen E, Starup J, Nielsen OH, Schwartz M, Drzewiecki KT, Mortensen EL, Main KM. Johannsen TH, et al. Among authors: schwartz m. Int J Pediatr Endocrinol. 2010;2010:784297. doi: 10.1155/2010/784297. Epub 2010 Oct 20. Int J Pediatr Endocrinol. 2010. PMID: 20981283 Free PMC article.

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