 Print previewpersonal data approved: 2023. VII. 05. | Publications |
2023
 from data base, 2023. V. 31. |
Hammer Anne Sofie Borg, Juul-Dam Kristian Løvvik, Sandahl Julie Damgaard, Abrahamsson Jonas, Czogala Malgorzata, Delabesse Emmanuelle, Haltrich Iren, Jahnukainen Kirsi, Kolb E. Anders, Kovács Gábor T, Leverger Guy, Locatelli Franco, Masetti Riccardo, Noren-Nystrom Ulrika, Raimondi Susana, Rasche Mareike, Reinhardt Dirk, Taki Tomohiko, Tomizawa Daisuke, Zeller Bernward, Hasle Henrik, Kjeldsen Eigil: Hypodiploidy has Unfavorable Impact on Survival in Pediatric Acute Myeloid Leukemia:An I-BFM Study Group collaboration, BLOOD ADVANCES 7: (6) pp. 1045-1055.
type of document:
language: English
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2022
from data base, 2023. V. 31. |
Szűcs Zsuzsanna, Pinti Éva, Haltrich Irén, Szén Orsolya Pálné, Nagy Tibor, Barta Endre, Méhes Gábor, Bidiga László, Török Olga, Ujfalusi Anikó, Koczok Katalin, Balogh István: An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 23: (21) 13076
type of document: Journal paper/Article
number of independent citations: 1
language: English
URL |
2022
from data base, 2023. V. 31. |
Lengyel Anna, Pinti Éva, Pikó Henriett, Kristóf Árvai, Abonyi Tünde, Némethi Zaránd, Fekete György, Haltrich Irén: Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohort, MOLECULAR CYTOGENETICS 15: (1) 47
type of document: Journal paper/Article
number of independent citations: 2
language: English
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2021
from data base, 2023. V. 31. |
Pinti Eva, Nemeth Krisztina, Staub Krisztina, Lengyel Anna, Fekete Gyorgy, Haltrich Iren: Diagnostic difficulties and possibilities of NF1-like syndromes in childhood, BMC PEDIATRICS 21: (1) 331
type of document: Journal paper/Article
number of independent citations: 7
language: English
URL |
2020
from data base, 2023. V. 31. |
Kiss Richárd, Gángó Ambrus, Benard-Slagter Anne, Egyed Bálint, Haltrich Irén, Hegyi Lajos, de Groot Karel, Király Péter Attila, Krizsán Szilvia, Kajtár Béla, Pikó Henriett, Pajor László, Vojcek Ágnes, Matolcsy András, Kovács Gábor, Szuhai Károly, Savola Suvi, Bödör Csaba, Alpár Donát: Comprehensive profiling of disease-relevant copy number aberrations for advanced clinical diagnostics of pediatric acute lymphoblastic leukemia, MODERN PATHOLOGY 33: (5) pp. 812-824.
type of document: Journal paper/Article
number of independent citations: 7
language: English
URL |
2020
from data base, 2023. V. 31. |
Eva Pinti, Anna Lengyel, Gyorgy Fekete, Iren Haltrich: What should we consider in the case of combined Down- and 47,XY,+i(X)(q10) Klinefelter syndromes? The unique case of a male newborn and review of the literature, BMC PEDIATRICS 20: 17
type of document: Journal paper/Review paper
number of independent citations: 6
language: English
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2020
from data base, 2023. V. 31. |
Lengyel Anna, Pinti Éva, Pikó Henriett, Jávorszky Eszter, David Dezső, Tihanyi Mariann, Gönczi Éva, Kiss Eszter, Tóth Zsuzsa, Tory Kálmán, Fekete György, Haltrich Irén: Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature, EUROPEAN JOURNAL OF MEDICAL GENETICS 63: (10) 104027
type of document: Journal paper/Article
number of independent citations: 2
language: English
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2019
from data base, 2023. V. 31. |
Hamadeh Lina, Enshaei Amir, Schwab Claire, Alonso Cristina N, Attarbaschi Andishe, Barbany Gisela, den Boer Monique L, Boer Judith M, Braun Marcin, Dalla Pozza Luciano, Elitzur Sarah, Emerenciano Mariana, Fechina Larisa, Felice Maria Sara, Fronkova Eva, Haltrich Irén, Heyman Mats M, Horibe Keizo, Imamura Toshihiko, Jeison Marta, Kovács Gábor, Kuiper Roland P, Mlynarski Wojciech, Nebral Karin, Ivanov Öfverholm Ingegerd, Pastorczak Agata, Pieters Rob, Piko Henriett, Pombo-de-Oliveira Maria S, Rubio Patricia, Strehl Sabine, Stary Jan, Sutton Rosemary, Trka Jan, Tsaur Grigory, Venn Nicola, Vora Ajay, Yano Mio, Harrison Christine J, Moorman Anthony V: Validation of the United Kingdom copy-number alteration classifier in 3239 children with B-cell precursor ALL, BLOOD ADVANCES 3: (2) pp. 148-157.
type of document:
number of independent citations: 28
language: English
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2014
from data base, 2023. V. 31. |
Blink M, Zimmermann M, Neuhoff CV, Reinhardt D, de Haas V, Hasle H, O' Brien MM, Stark B, Tandonnet J, Pession A, Tousovska K, Cheuk DK, Kudo K, Taga T, Rubnitz JE, Haltrich I, Balwierz W, Pieters R, Forestier E, Johansson B, van den Heuvel-Eibrink MM, Zwaan CM: Normal karyotype is a poor prognostic factor in Myeloid Leukemia of Down Syndrome: a retrospective international study, HAEMATOLOGICA 99: (2) pp. 299-307.
type of document: Journal paper/Article
number of independent citations: 26
language: English
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2014
from data base, 2023. V. 31. |
Harrison CJ, Moorman AV, Schwab C, Carroll AJ, Raetz EA, Devidas M, Strehl S, Nebral K, Harbott J, Teigler-Schlegel A, Zimmerman M, Dastuge N, Baruchel A, Soulier J, Auclerc MF, Attarbaschi A, Mann G, Stark B, Cazzaniga G, Chilton L, Vandenberghe P, Forestier E, Haltrich I, Raimondi SC, Parihar M, Bourquin JP, Tchinda J, Haferlach C, Vora A, Hunger SP, Heerema NA, Ponte di Legno International Workshop in Childhood Acute Lymphoblastic Leukemia, Haas OA: An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome, LEUKEMIA 28: (5) pp. 1015-1021.
type of document:
number of independent citations: 164
language: English
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| | Number of independent citations to these publications: | 243 |
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