161 related articles for article (PubMed ID: 9440957)
1. [Sialidosis and galactosialidosis as the cause of non-immunologic hydrops fetalis].
Schmidt M; Fahnenstich H; Haverkamp F; Platz H; Hansmann M; Bartmann P
Z Geburtshilfe Neonatol; 1997; 201(5):177-80. PubMed ID: 9440957
[TBL] [Abstract][Full Text] [Related]
2. Hydrops fetalis in four siblings caused by galactosialidosis.
Landau D; Meisner I; Zeigler M; Bargal R; Shinwell ES
Isr J Med Sci; 1995 May; 31(5):321-2. PubMed ID: 7759227
[No Abstract] [Full Text] [Related]
3. Sialidosis and galactosialidosis: chromosomal assignment of two genes associated with neuraminidase-deficiency disorders.
Mueller OT; Henry WM; Haley LL; Byers MG; Eddy RL; Shows TB
Proc Natl Acad Sci U S A; 1986 Mar; 83(6):1817-21. PubMed ID: 3081902
[TBL] [Abstract][Full Text] [Related]
4. Nonimmune hydrops fetalis with galactosialidosis: consequences for family planning.
Haverkamp F; Jacobs D; Cantz M; Hansmann M; Fahnenstich H; Zerres K
Fetal Diagn Ther; 1996; 11(2):114-9. PubMed ID: 8838767
[TBL] [Abstract][Full Text] [Related]
5. Galactosialidosis presenting as nonimmune fetal hydrops: a case report.
Carvalho S; Martins M; Fortuna A; Ramos U; Ramos C; Rodrigues MC
Prenat Diagn; 2009 Sep; 29(9):895-6. PubMed ID: 19466716
[No Abstract] [Full Text] [Related]
6. Refractory congenital ascites as a manifestation of neonatal sialidosis: clinical, biochemical and morphological studies in a newborn Syrian male infant.
Sergi C; Beedgen B; Kopitz J; Zilow E; Zoubaa S; Otto HF; Cantz M; Linderkamp O
Am J Perinatol; 1999; 16(3):133-41. PubMed ID: 10438195
[TBL] [Abstract][Full Text] [Related]
7. A case of galactosialidosis with a homozygous Q49R point mutation.
Matsumoto N; Gondo K; Kukita J; Higaki K; Paragison RC; Nanba E
Brain Dev; 2008 Oct; 30(9):595-8. PubMed ID: 18396002
[TBL] [Abstract][Full Text] [Related]
8. Lysosomal storage disease spectrum in nonimmune hydrops fetalis: a retrospective case control study.
Al-Kouatly HB; Felder L; Makhamreh MM; Kass SL; Vora NL; Berghella V; Berger S; Wenger DA; Luzi P
Prenat Diagn; 2020 May; 40(6):738-745. PubMed ID: 32134517
[TBL] [Abstract][Full Text] [Related]
9. Lysosomal storage diseases presenting as transient or persistent hydrops fetalis.
Bonduelle M; Lissens W; Goossens A; De Catte L; Foulon W; Denis R; Jauniaux E; Liebaers I
Genet Couns; 1991; 2(4):227-32. PubMed ID: 1799421
[TBL] [Abstract][Full Text] [Related]
10. Case Records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 23-1997. A premature newborn infant with congenital ascites.
N Engl J Med; 1997 Jul; 337(4):260-7. PubMed ID: 9227933
[No Abstract] [Full Text] [Related]
11. [Nonimmunologic hydrops fetalis--a review of 31 cases].
Schmid G; Fahnenstich H; Redel D; Gembruch U; Niesen M; Kowalewski S
Klin Padiatr; 1988; 200(4):287-93. PubMed ID: 3172669
[TBL] [Abstract][Full Text] [Related]
12. De novo reciprocal translocation t(5;11)(q22;p15) associated with hydrops fetalis (reciprocal translocation and hydrops fetalis).
Pala HG; Artunc-Ulkumen B; Uyar Y; Bal F; Baytur YB; Koyuncu FM
Fetal Pediatr Pathol; 2015 Feb; 34(1):44-8. PubMed ID: 25289481
[TBL] [Abstract][Full Text] [Related]
13. Neuraminidase deficiency presenting as non-immune hydrops fetalis.
Beck M; Bender SW; Reiter HL; Otto W; Bässler R; Dancygier H; Gehler J
Eur J Pediatr; 1984 Dec; 143(2):135-9. PubMed ID: 6240403
[TBL] [Abstract][Full Text] [Related]
14. [Primary neuraminidase deficiency with prenatal disclosure].
Tabardel Y; Soyeur D; Vivario E; Senterre J
Arch Fr Pediatr; 1989 Dec; 46(10):737-40. PubMed ID: 2697196
[TBL] [Abstract][Full Text] [Related]
15. Sialidosis presenting as severe nonimmune fetal hydrops is associated with two novel mutations in lysosomal alpha-neuraminidase.
Loren DJ; Campos Y; d'Azzo A; Wyble L; Grange DK; Gilbert-Barness E; White FV; Hamvas A
J Perinatol; 2005 Jul; 25(7):491-4. PubMed ID: 15908988
[TBL] [Abstract][Full Text] [Related]
16. Nonimmune hydrops fetalis diagnosed during the second half of pregnancy in Southern China.
Liao C; Wei J; Li Q; Li J; Li L; Li D
Fetal Diagn Ther; 2007; 22(4):302-5. PubMed ID: 17361085
[TBL] [Abstract][Full Text] [Related]
17. Lysosomal storage disorders as an etiology of nonimmune hydrops fetalis: A systematic review.
Iyer NS; Gimovsky AC; Ferreira CR; Critchlow E; Al-Kouatly HB
Clin Genet; 2021 Nov; 100(5):493-503. PubMed ID: 34057202
[TBL] [Abstract][Full Text] [Related]
18. Investigation of lysosomal storage diseases in nonimmune hydrops fetalis.
Burin MG; Scholz AP; Gus R; Sanseverino MT; Fritsh A; Magalhães JA; Timm F; Barrios P; Chesky M; Coelho JC; Giugliani R
Prenat Diagn; 2004 Aug; 24(8):653-7. PubMed ID: 15305357
[TBL] [Abstract][Full Text] [Related]
19. [Prenatal diagnosis of sialidosis, a defect of the lysosomal enzyme neuraminidase].
Heyes H; Gehler J; Töllner U; Göltner E
Geburtshilfe Frauenheilkd; 1988 Nov; 48(11):814-5. PubMed ID: 3234713
[TBL] [Abstract][Full Text] [Related]
20. [Sialidosis].
Kobayashi T; Kuroiwa Y
Nihon Rinsho; 1986 Jul; 44(7):1671-6. PubMed ID: 3093734
[No Abstract] [Full Text] [Related]
[Next] [New Search]