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Nivin Moustafa-Hawash
Observed names:
Moustafa Nivin,
Nivin Hawash-Moustafa,
Nivin Moustafa,
Nivin moustafa-Hawash
Institution:
Rambam Health Care Campus
Observed institutions:
Tel Aviv University,
Sheba Medical Center,
Rambam Health Care Campus,
Meir Medical Center,
Meyer Children's Hospital
OpenAlex ID:
A5076337128
A Nonsense Mutation in the Human Homolog of Drosophila rogdi Causes Kohlschutter–Tonz Syndrome
2012
·
Adi Mory
, Efrat Dagan
, et al.
·
The American Journal of Human Genetics
·
30
PDF
Superior outcome of patients with favorable-risk acute myeloid leukemia using consolidation with autologous stem cell transplantation
2019
·
Ofrat Beyar-Katz
, Noa Lavi
, et al.
·
Leukemia & lymphoma/Leukemia and lymphoma
·
14
Homozygosity for CHEK2 p.Gly167Arg leads to a unique cancer syndrome with multiple complex chromosomal translocations in peripheral blood karyotype
2019
·
Tamar Paperna
, Nitzan Sharon-Shwartzman
, et al.
·
Journal of Medical Genetics
·
13
‘Pure’ partial trisomy 11q (11q23.1→11qter)
2011
·
Avishag Zimberg-Bossira
, Tatiana Smolkin
, et al.
·
Clinical Dysmorphology
·
12
ERK Activity in Immature Leukemic Cells Drives Clonal Selection during Induction Therapy for Acute Myeloid Leukemia
2020
·
Michal Hayun
, Maria Zaatra
, et al.
·
Scientific Reports
·
9
PDF
CHARGE syndrome with del(3)(p13p21): expanding the genotype.
2012
·
Nivin Moustafa-Hawash
, Tatiana Smolkin
, et al.
·
PubMed
·
3
Aberration of 3q and monosomy 7 in a child with acute myelogenous leukemia
2007
·
Motti Haimi
, Ronit Elhasid
, et al.
·
Cancer Genetics and Cytogenetics
·
3
Treatment-related acute myeloid leukemia characterized by t(11;20)(p15;q11) and del(9)(q22)
2006
·
Haimi Motti
, Avivi Irit
, et al.
·
Cancer Genetics and Cytogenetics
·
3
Spontaneous Remission of Childhood Acute Marrow Fibrosis and Megakaryoblastic Leukemia
2012
·
Ronit Elhasid
, Tali Tohami
, et al.
·
Journal of Pediatric Hematology/Oncology
·
2
Optical Genome Mapping Reclassifies Patients with Intermediate Risk Acute Myeloid Leukemia
2024
·
Baher Krayem
, Nivin moustafa-Hawash
, et al.
·
Blood
·
1
PDF
The d3GHR carrier epigenome in Druze clan longevity
2024
·
Ghadeer Falah
, Alina Kurolap
, et al.
·
Scientific Reports
·
1
PDF
Missense substitutions in the BTB domain of ZBTB24 can lead to protein instability and cause ICF2 syndrome
2025
·
Or Givol
, Ido S Han
, et al.
·
Human Molecular Genetics
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Works count:
12
Citation count:
91
H-index:
5
I10-index:
4
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