I. Hainmann

发表

Recurring mutations in RPL15 are linked to hydrops fetalis and treatment independence in Diamond-Blackfan anemia

M. Wlodarski, A. MacInnes, L. D. Da Costa, 2018, Haematologica.

Diagnosis and management of chronic ITP: comments from an ICIS expert group

I. Hainmann, A. Tichelli, Mohsen Saleh Elalfy, 2010, Annals of Hematology.

Isolation of new splice isoforms, characterization and expression analysis of the human septin SEPT8 (KIAA0202).

I. Hainmann, B. Zieger, S. Bläser, 2003, Gene.

High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9

R. Pieters, I. Hainmann, J. Meijerink, 2006, Genes, chromosomes & cancer.

Diamond-Blackfan Anemia Phenotype Caused By Deficiency of Adenosine Deaminase 2

K. Schwarz, D. Steinemann, S. Ehl, 2017 .

Successful ECMO therapy in a child with COVID‐19‐associated ARDS and acute lymphoblastic leukemia

I. Hainmann, H. Reutter, A. Müller, 2021, Pediatric blood & cancer.

Functional flow cytometry of monocytes for routine diagnosis of innate primary immunodeficiencies.

S. Ehl, S. Fuchs, I. Hainmann, 2019, The Journal of allergy and clinical immunology.

Progressive Thrombosis in a 13-Year-Old Girl with Trisomy 21 Under Therapy with Low Molecular Weight Heparin

I. Hainmann, A. Karow, U. Budde, 2011, Klinische Pädiatrie.

Medullary haemorrhage of the femur as presenting sign of haemophilia in a 22‐month‐old boy

I. Hainmann, M. Uhl, B. Zieger, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

Novel findings in two patients with late‐diagnosed afibrinogenaemia: intraosseous haemorrhage and fingertip necrosis

J. Heiss, J. Oldenburg, I. Hainmann, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification of a novel factor X deletion in combination with a missense mutation in the F10 gene

J. Oldenburg, I. Hainmann, A. Pavlova, 2009, Hämostaseologie.

Favorable outcomes of hematopoietic stem cell transplantation in children and adolescents with Diamond-Blackfan anemia.

B. Burkhardt, A. Schulz, M. Wlodarski, 2020, Blood advances.

Molecular Genetic Analysis of a Patient with Moderate Hemophilia A and Psychomotor Developmental Delay

J. Oldenburg, I. Hainmann, S. Rost, 2013, Klinische Pädiatrie.

Deletion of human GP 1 BB and SEPT 5 is associated with Bernard-Soulier syndrome , platelet secretion defect , polymicrogyria , and develop-mental delay

P. Nurden, J. Oldenburg, I. Hainmann, 2018 .

Human septin–septin interaction: CDCrel‐1 partners with KIAA0202

I. Hainmann, B. Zieger, A. Zgaga-Griesz, 2002, FEBS letters.

The expansion of human T-bethighCD21low B cells is T cell dependent

J. Casanova, M. Boerries, M. van der Burg, 2021, Science Immunology.

Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency

J. Casanova, R. Badolato, R. Fuleihan, 2021, The Journal of Immunology.

Characterization and expression analysis of two human septin genes, PNUTL1 and PNUTL2.

I. Hainmann, J. Ware, B. Zieger, 2000, Gene.

Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay

P. Nurden, J. Oldenburg, I. Hainmann, 2011, Thrombosis and Haemostasis.

The novel human platelet septin SEPT8 is an interaction partner of SEPT4

P. Nurden, I. Hainmann, A. Pagenstecher, 2004, Thrombosis and Haemostasis.

Compound Heterozygous Mutations in 2 Siblings with Hermansky-Pudlak Syndrome Type 1 (HPS1)

I. Hainmann, B. Zieger, I. Bartsch, 2010, Klinische Padiatrie.

Compound Heterozygosity of the Protein S-Gene as a Cause of Severe Cerebral Sinovenous Thrombosis in a 7-Year-Old Child

I. Mader, J. Oldenburg, I. Hainmann, 2010, Klinische Padiatrie.