183 related articles for article (PubMed ID: 35321730)
21. Pulmonary interstitial glycogenosis in the setting of lung growth abnormality: radiographic and pathologic correlation.
Castillo M; Vade A; Lim-Dunham JE; Masuda E; Massarani-Wafai R
Pediatr Radiol; 2010 Sep; 40(9):1562-5. PubMed ID: 20440487
[TBL] [Abstract][Full Text] [Related]
22. Pulmonary interstitial glycogenosis in a patient ultimately diagnosed with Noonan syndrome.
Ross MK; Ellis LS; Bird LM; Hagood JS
Pediatr Pulmonol; 2014 May; 49(5):508-11. PubMed ID: 24039098
[TBL] [Abstract][Full Text] [Related]
23. Pulmonary growth abnormalities as etiologies for pediatric pulmonary hypertension.
Mallory GB; Spielberg DR; Silva-Carmona M
Pediatr Pulmonol; 2021 Mar; 56(3):678-685. PubMed ID: 32735399
[TBL] [Abstract][Full Text] [Related]
24. Diagnostic and clinical course of pulmonary interstitial glycogenosis: The tip of the iceberg.
Yonker LM; Kinane TB
Pediatr Pulmonol; 2018 Dec; 53(12):1659-1661. PubMed ID: 30259700
[TBL] [Abstract][Full Text] [Related]
25. 11q terminal deletion and combined immunodeficiency (Jacobsen syndrome): Case report and literature review on immunodeficiency in Jacobsen syndrome.
Blazina Š; Ihan A; Lovrečić L; Hovnik T
Am J Med Genet A; 2016 Dec; 170(12):3237-3240. PubMed ID: 27605496
[TBL] [Abstract][Full Text] [Related]
26. Successful surgical repair of a massive window duct in a 1-month old with aniridia and pulmonary interstitial glycogenosis.
Siomos AK; Mitchell MB; Fonseca BM
Cardiol Young; 2015 Mar; 25(3):594-6. PubMed ID: 24848376
[TBL] [Abstract][Full Text] [Related]
27. Jacobsen syndrome: Advances in our knowledge of phenotype and genotype.
Favier R; Akshoomoff N; Mattson S; Grossfeld P
Am J Med Genet C Semin Med Genet; 2015 Sep; 169(3):239-50. PubMed ID: 26285164
[TBL] [Abstract][Full Text] [Related]
28. Persistent Tachypnea of Infancy. Usual and Aberrant.
Rauch D; Wetzke M; Reu S; Wesselak W; Schams A; Hengst M; Kammer B; Ley-Zaporozhan J; Kappler M; Proesmans M; Lange J; Escribano A; Kerem E; Ahrens F; Brasch F; Schwerk N; Griese M;
Am J Respir Crit Care Med; 2016 Feb; 193(4):438-47. PubMed ID: 26474448
[TBL] [Abstract][Full Text] [Related]
29. Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocation.
Chen CP; Lin SP; Hsu CH; Chern SR; Su JW; Chen YJ; Pan CW; Wang W
Genet Couns; 2012; 23(2):223-9. PubMed ID: 22876581
[TBL] [Abstract][Full Text] [Related]
30. Brain hemorrhages in Jacobsen syndrome: A retrospective review of six cases and clinical recommendations.
Grossfeld P
Am J Med Genet A; 2017 Mar; 173(3):667-670. PubMed ID: 28211970
[TBL] [Abstract][Full Text] [Related]
31. Ventriculomegaly and cerebellar hypoplasia in a neonate with interstitial 11q 24 deletion in Jacobsen syndrome region.
Puvabanditsin S; Chen CW; Botwinick M; Hussein K; Mariduena J; Mehta R
Clin Case Rep; 2018 Jul; 6(7):1268-1275. PubMed ID: 29988670
[TBL] [Abstract][Full Text] [Related]
32. Ultrastructural characterization of genetic diffuse lung diseases in infants and children: a cohort study and review.
Citti A; Peca D; Petrini S; Cutrera R; Biban P; Haass C; Boldrini R; Danhaive O
Ultrastruct Pathol; 2013 Oct; 37(5):356-65. PubMed ID: 24047351
[TBL] [Abstract][Full Text] [Related]
33. Pulmonary interstitial glycogenosis: words of caution.
Deutsch GH; Young LR
Pediatr Radiol; 2010 Sep; 40(9):1471-5. PubMed ID: 20593171
[No Abstract] [Full Text] [Related]
34. Jacobsen syndrome.
Mattina T; Perrotta CS; Grossfeld P
Orphanet J Rare Dis; 2009 Mar; 4():9. PubMed ID: 19267933
[TBL] [Abstract][Full Text] [Related]
35. 11q23 deletion syndrome (Jacobsen syndrome) with severe bleeding: a case report.
Ichimiya Y; Wada Y; Kunishima S; Tsukamoto K; Kosaki R; Sago H; Ishiguro A; Ito Y
J Med Case Rep; 2018 Jan; 12(1):3. PubMed ID: 29307309
[TBL] [Abstract][Full Text] [Related]
36. Irreversible Respiratory Failure in a Full-Term Infant with Features of Pulmonary Interstitial Glycogenosis as Well as Bronchopulmonary Dysplasia.
Jiskoot-Ermers ME; Antonius TA; Looijen-Salamon MG; Wijnen MH; Loza BF; Heijst AF
AJP Rep; 2015 Oct; 5(2):e136-40. PubMed ID: 26495172
[TBL] [Abstract][Full Text] [Related]
37. De novo interstitial deletion in the long arm of chromosome 11: a case report.
Li LL; Zhang HG; Shao XG; Gao JC; Zhang HY; Liu RZ
Genet Mol Res; 2016 Jul; 15(2):. PubMed ID: 27421024
[TBL] [Abstract][Full Text] [Related]
38. The 11q Terminal Deletion Disorder Jacobsen Syndrome is a Syndromic Primary Immunodeficiency.
Dalm VA; Driessen GJ; Barendregt BH; van Hagen PM; van der Burg M
J Clin Immunol; 2015 Nov; 35(8):761-8. PubMed ID: 26566921
[TBL] [Abstract][Full Text] [Related]
39. Congenital interstitial lung diseases: What the anesthesiologist needs to know.
Bertolizio G; Engelhardt T; Veyckemans F
Paediatr Anaesth; 2022 Feb; 32(2):138-147. PubMed ID: 34738691
[TBL] [Abstract][Full Text] [Related]
40. Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice.
Ye M; Coldren C; Liang X; Mattina T; Goldmuntz E; Benson DW; Ivy D; Perryman MB; Garrett-Sinha LA; Grossfeld P
Hum Mol Genet; 2010 Feb; 19(4):648-56. PubMed ID: 19942620
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]