Malgorzata Piotrowicz
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Explore the profile of Malgorzata Piotrowicz including associated specialties, affiliations and a list of published articles.
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23
Citations
156
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Recent Articles
11.
Mlynarski E, Xie M, Taylor D, Sheridan M, Guo T, Racedo S, et al.
Hum Genet
. 2016 Jan;
135(3):273-85.
PMID: 26742502
The 22q11.2 deletion syndrome (22q11DS; velocardiofacial/DiGeorge syndrome; VCFS/DGS; MIM #192430; 188400) is the most common microdeletion syndrome. The phenotypic presentation of 22q11DS is highly variable; approximately 60-75 % of 22q11DS...
12.
Mlynarski E, Sheridan M, Xie M, Guo T, Racedo S, McDonald-McGinn D, et al.
Am J Hum Genet
. 2015 Apr;
96(5):753-64.
PMID: 25892112
The 22q11.2 deletion syndrome (22q11DS; velocardiofacial/DiGeorge syndrome; VCFS/DGS) is the most common microdeletion syndrome and the phenotypic presentation is highly variable. Approximately 65% of individuals with 22q11DS have a congenital...
13.
Gos M, Fahiminiya S, Poznanski J, Klapecki J, Obersztyn E, Piotrowicz M, et al.
Am J Med Genet A
. 2014 Jun;
164A(9):2310-6.
PMID: 24939608
No abstract available.
14.
Kolecka E, Niedzielski K, Cukras Z, Piotrowicz M
Chir Narzadow Ruchu Ortop Pol
. 2012 Mar;
76(5):252-5.
PMID: 22420177
Although congenital talipes equinovarus (CTEV) is one of the most frequently occurring congenital defects of locomotor organs, its ethiopathogenesis is still not fully known. Amongst the others, the inheritance patterns...
15.
Rotsztejn H, Czkwianianc E, Juchniewicz B, Piotrowicz M, Wendorff J
Med Wieku Rozwoj
. 2009 Aug;
13(1):49-52.
PMID: 19648660
Peutz-Jeghers syndrome is an autosomal dominant inherited disorder which is characterized by mucocutaneus melanocytic macules and intestinal hamartomatous polypus. The aim of our work is to underline the role of...
16.
Rotsztejn H, Juchniewicz B, Piotrowicz M, Wendorff J, Czkwianianc E
Pol Merkur Lekarski
. 2009 Apr;
26(151):86-8.
PMID: 19391516
The aim of our study is to introduce a larger number of doctors to the subject of lentigines. They may be a first syndrome coexistent with very rare multiple organ...
17.
Pasnik J, Cywinska-Bernas A, Piotrowicz M
Postepy Hig Med Dosw (Online)
. 2007 Jun;
61:361-8.
PMID: 17572656
The 22q11.2 deletion syndrome occurs in approximately 1 of 3000-5000 children. This is a congenital disorder characterized by facial dysmorphic features, cardiac defects, thymic hypoplasia, cleft palate, hypoparathyroidism, and psychiatric...
18.
Kamer B, Rotsztejn H, Kulig A, Raczynska J, Piotrowicz M, Kulig K, et al.
Pol Merkur Lekarski
. 2005 Dec;
19(112):542-4.
PMID: 16379321
The coexistence of atopic dermatitis and psoriasis is especially rare diagnosed disease in small children. Authors present a 12 months-old girl with both of these diseases. It is important to...
19.
Nowicki G, Alaszewski W, Kudra A, Szaflik K, Potrzebowska A, Piotrowicz M
Ginekol Pol
. 2004 Apr;
75(2):119-23.
PMID: 15108583
Objectives: To determine whether it is fetal blood and not with mother blood in question. Design: We discuss the "Apt test" results which examines the fetal hemoglobin in blood samples...
20.
Janiak K, Kaczmarek P, Krason A, Nowicki G, Piotrowicz M, Respondek-Liberska M
Ginekol Pol
. 2002 Oct;
73(7):606-12.
PMID: 12369282
Objective: Assessment of usefulness of the fetal echocardiography and genetic sonography in prenatal diagnosis trisomy 13 (retrospective analysis). Material And Method: Between 1994-1999 at the Department for Diagnosis of Congenital...