I. Šubrt

发表

Prospective study on the relationship between cervical neoplasia and herpes simplex type‐2 virus. I. Epidemiological characteristics

V. Dvorakova, I. Hirsch, J. Jelínek, 1984, International journal of cancer.

The prevalence of cancer in patients with superficial vein thrombosis and its clinical importance.

J. Seidlerová, J. Hirmerová, I. Šubrt, 2021, Journal of vascular surgery. Venous and lymphatic disorders.

ORIGINAL ARTICLE: Urgent Termination of Pregnancy in Pre‐eclampsia and Panel of Antiphospholipid Antibodies

Z. Ulčová-Gallová, L. Hradecký, I. Šubrt, 2009, American journal of reproductive immunology.

Six new gap junction beta 1 gene mutations and their phenotypic expression in Czech patients with Charcot-Marie-Tooth disease.

P. Seeman, R. Mazanec, J. Haberlová, 2010, Genetic testing and molecular biomarkers.

Recurrent Pregnancy Loss, Plasminogen Activator Inhibitor‐1 (‐675) 4G/5G Polymorphism and Antiphospholipid Antibodies in Czech Women

Z. Ulčová-Gallová, I. Šubrt, M. Černá, 2013, American journal of reproductive immunology.

Multiclonal monoallelic 13q14 interstitial deletion in chronic lymphocytic leukemia

I. Šubrt, M. Hruba, 2013, Leukemia & lymphoma.

The association of factor V Leiden with various clinical patterns of venous thromboembolism-the factor V Leiden paradox.

J. Seidlerová, J. Hirmerová, I. Šubrt, 2014, QJM : monthly journal of the Association of Physicians.

the factor V Leiden paradox

J. Hirmerová, I. Šubrt, Jitka Mlíková-Seidlerová, 2014 .

The translocation t(2;11)(p21;q23) without MLL gene rearrangement—a possible marker of good prognosis in myelodysplastic syndrome patients

K. Michalová, P. Dvořák, D. Lysák, 2014, Hematological oncology.

Fenofibrate-induced hyperhomocysteinemia may be prevented by folate co-administration

O. Mayer, L. Holubec, J. Šimon, 2003, European Journal of Clinical Pharmacology.

The effects of folate supplementation on some coagulation parameters and oxidative status surrogates

O. Mayer, M. Hromadka, H. Rosolová, 2002, European Journal of Clinical Pharmacology.

Cytokine Tumor Necrosis Factor-alpha A Promoter Gene Polymorphism at Position −308 G→A and Pediatric Inflammatory Bowel Disease: Implications in Ulcerative Colitis and Crohn's Disease

K. Siala, J. Varvařovská, J. Sýkora, 2006, Journal of pediatric gastroenterology and nutrition.

Deep vein thrombosis and/or pulmonary embolism concurrent with superficial vein thrombosis of the legs: cross-sectional single center study of prevalence and risk factors.

J. Seidlerová, J. Hirmerová, I. Šubrt, 2013, International angiology : a journal of the International Union of Angiology.

Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11

D. Page, A. Chapelle, C. Turleau, 1988, Human Genetics.

ORIGINAL ARTICLE: Recurrent Pregnancy Loss and Frequency of Eight Antiphospholipid Antibodies and Genetic Thrombophilic Factors in Czech Women

Z. Novotný, Z. Ulčová-Gallová, L. Hradecký, 2008, American journal of reproductive immunology.

A further example of familial Gp+ associated with trisomy G

I. Šubrt, 2004, Humangenetik.

First case report of rare congenital adrenal insufficiency caused by mutations in the CYP11A1 gene in the Czech Republic

J. Varvařovská, R. Pomahačová, J. Sýkora, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Robertsonian translocation between the chromosome Y and 15

I. Šubrt, B. Blehová, 1974, Humangenetik.

45,X/47,XYY mosaicism: clinical discrepancy between prenatally and postnatally diagnosed cases.

B. Burton, S. Kahler, M. Wheeler, 1991, American journal of medical genetics.

CHROMOSOMES IN ALBRIGHT'S SYNDROME

I. Šubrt, V. Brychnáč, 1966 .

Aberrant chromosome 13-15 in a patient with Down's syndrome, diabetes mellitus and hyperthyroidism and in his father.

I. Šubrt, B. Blehová, J. Kucera, 1968, Acta genetica et statistica medica.

Cytogenetic study of cleft lip and palate.

J. Cervenka, I. Šubrt, M. Krecek, 1966, The Cleft palate journal.

Mewing cry in a child with the partial deletion of the short arm of chromosome No. 4

E. Sedláčková, I. Šubrt, B. Blehová, 2004, Humangenetik.

The 11q;22q translocation: A European collaborative analysis of 43 cases

C. E. Ford, G. Gimelli, A. Hagemeijer, 2004, Human Genetics.

Trisomy 9p resulting from maternal 9/21 translocation

I. Šubrt, B. Blehová, B. Pallová, 1976, Human Genetics.

Late diagnosis of complete androgen insensitivity syndrome and transmission/carriers of the disease in a family with mutation c.2495G>T p.(Arg832Leu) in exon 7 of the androgen receptor gene: genetic, clinical and ethical aspects.

R. Pomahačová, J. Sýkora, A. Křepelová, 2019, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.

Independent coexistence of clones with 13q14 deletion at reciprocal translocation breakpoint and 13q14 interstitial deletion in chronic lymphocytic leukemia

P. Dvořák, Lucie Weberová, I. Šubrt, 2012, Leukemia & lymphoma.

Familial translocation t(17;22), including the segregation in five consecutive abortuses

I. Šubrt, K. Štirská, 1988, Human Genetics.

Reciprocal translocation with special reference to reproductive failure

I. Šubrt, 2004, Human Genetics.

Dicentric chromosome due to an unusual fusion

I. Šubrt, B. Blehová, O. Táborský, 2004, Humangenetik.

Further observations on a previously reported case of 4p-syndrome

I. Šubrt, B. Blehová, 1972, Humangenetik.

Double chromosomal aberration

I. Šubrt, H. Prchlíková, 1969, Humangenetik.

Phenylketonuria associated with Down's syndrome.

I. Šubrt, B. Blehová, N. Pažoutová, 2008, Journal of mental deficiency research.

Partial trisomy 9q- chromosomal syndrome

I. Šubrt, J. Jodl, M. Janovsky, 1976, Human Genetics.

Leukaemia inhibitory factor (LIF) gene mutations in women diagnosed with unexplained infertility and endometriosis have a negative impact on the IVF outcome. A pilot study.

P. Šíma, Z. Novotný, M. Králíčková, 2009, Folia biologica.

Microdensitometric identification of the pericentric inversion of chromosome No.2 and of duplication of the short arm of chromosome No.7 in a reexamined case.

O. Hníková, I. Šubrt, J. Kozák, 1973, Human heredity.

A case of the 18p—Syndrome

I. Šubrt, J. Beránková, 2004, Humangenetik.

Familial occurrence of 18q-

J. Pokorný, I. Šubrt, 1970, Humangenetik.

Trisomy for short arm of chromosome 20

I. Šubrt, V. Brychnáč, 2004, Humangenetik.

Development of acute myeloid leukemia associated with Ph-negative clone with inv(3)(q21q26) during imatinib therapy for chronic myeloid leukemia.

P. Dvořák, I. Šubrt, M. Hruba, 2009, Leukemia research.

Terrorism as a slap in the face of the civilized world

K. Černý, I. Šubrt, K. Černý, 2016 .

Post-mortem genetic testing in sudden cardiac death and genetic screening of relatives at risk: lessons learned from a Czech pilot multidisciplinary study

J. Kautzner, P. Tomášek, Jakub Stocek, 2023, International Journal of Legal Medicine.

(Postmortem genetic testing in sudden cardiac death victims and genetic screening of relatives at risk in the Czech Republic)

J. Kautzner, P. Tomášek, M. Kulvajtová, 2023, Cor et Vasa.

First 2 cases with thiamine‐responsive megaloblastic anemia in the Czech Republic, a rare form of monogenic diabetes mellitus: a novel mutation in the thiamine transporter SLC19A2 gene—intron 1 mutation c.204+2T>G

P. Jehlička, R. Pomahačová, J. Sýkora, 2017, Pediatric diabetes.

Precise determination of primary cytogenetic abnormalities provides added value for stratification of chronic lymphocytic leukemia patients.

P. Dvořák, D. Lysák, I. Šubrt, 2019, Neoplasma.

ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

James M. Hodge, E. Burnside, Y. Kamatani, 2023, Clinical cancer research : an official journal of the American Association for Cancer Research.

Sol-gel derived iron oxide-silica nanocomposites, starting from iron chloride and iron nitrate

M. Popovici, C. Savii, C. Enache, 2005 .

Fatco syndrome (fibular Aplasia, tibial campomelia and oligosyndactyly)

V. Vyskočil, Z. Chudáček, I. Šubrt, 2010 .

Lynch syndrome-associated upper tract urothelial carcinoma frequently occurs in patients older than 60 years: an opportunity to revisit urology clinical guidelines.

R. Alaghehbandan, O. Hes, M. Hora, 2023, Virchows Archiv : an international journal of pathology.

Cystic ovarian teratoma as a novel tumor and growth hormone deficiency as new conditions presenting in Multiple Endocrine Neoplasia type 2B: Case reports and review of the literature.

R. Pomahačová, J. Sýkora, R. Katra, 2021, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.

Recurrent Pregnancy Loss, Plasminogen Activator Inhibitor‐1 (‐675) 4G/5G Polymorphism and Antiphospholipid Antibodies in Czech Women

Z. Ulčová-Gallová, I. Šubrt, M. Černá, 2013, American journal of reproductive immunology.

Prenatal diagnosis of bloody amniotic fluid.

I. Šubrt, 1987, American journal of medical genetics.