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1

Euro-Area Quantitative Easing and Portfolio Rebalancing

Koijen, Ralph S. J., Koulischer, François, Nguyen, Benoît, Yogo, Motohiro

Journal:

American Economic Review

Year:

2017

Language:

english

File:

PDF, 465 KB

english, 2017

2

Central bank liquidity provision and collateral quality

Koulischer, François, Struyven, Daan

Journal:

Journal of Banking & Finance

Year:

2014

Language:

english

File:

PDF, 972 KB

english, 2014

3

Inspecting the mechanism of quantitative easing in the euro area

Koijen, Ralph S.J., Koulischer, FranÃ§ois, Nguyen, BenoÃ®t, Yogo, Motohiro

Journal:

Journal of Financial Economics

Year:

2020

File:

PDF, 3.29 MB

2020

4

Monosomy 11q: Report of two familial cases and review of the literature

Roland Hustinx, Dr. Alian Verloes, Bettina Grattagliano, Christian Herens, Mauricette Jamar, Danial Soyeur, Jean-Pierre Schaaps, Lucien Koulischer

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 613 KB

english, 1993

5

A prenatal trisomy 21 screening program using α-fetoprotein, human chorionic gonadotropin, and free estriol assays on maternal dried blood

Alain Verloes, Roland Schoos, Christian Herens, Anne Vintens, Lucien Koulischer

Journal:

American Journal of Obstetrics and Gynecology

Year:

1995

Language:

english

File:

PDF, 809 KB

english, 1995

6

Degradation of cholecystokinin octapeptide, related fragments and analogs by human and rat plasma in vitro

Koulischer, Denis, Moroder, Luis, Deschodt-Lanckman, Monique

Journal:

Regulatory Peptides

Year:

1982

Language:

english

File:

PDF, 653 KB

english, 1982

7

Quantitative Easing in the Euro Area: The Dynamics of Risk Exposures and the Impact on Asset Prices.

Koijen, Ralph S. J., Koulischer, Francois, Nguyen, Benoot, Yogo, Motohiro

Journal:

SSRN Electronic Journal

Year:

2016

File:

PDF, 327 KB

2016

8

Microcephaly, muscular build, rhizomelia, and cataracts: Description of a possible recessive syndrome and some comments on the use of electronic databases in syndromology

Verloes, Alain, Lesenfants, Sylviane, Misson, Jean-Paul, Galand, Albert, Koulischer, Lucien

Journal:

American Journal of Medical Genetics

Year:

1997

File:

PDF, 16.10 MB

1997

9

Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form

Verloes, Alain, Massin, Martial, Lombet, Jacques, Grattagliano, Bettina, Soyeur, Daniel, Rigo, Jacques, Koulischer, Lucien, Van Hoof, François

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 256 KB

english, 1997

10

Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome

Herens, Christian, Jamar, Mauricette, Alvarez-Gonzalez, Maria-Luz, Lesenfants, Sylviane, Lombet, Jacques, Bonnivert, Jacqueline, Koulischer, Lucien, Verloes, Alain

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 208 KB

english, 1997

11

Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases

Jacques Poncin, Roger Abs, Brigitte Velkeniers, Maryse Bonduelle, Marc Abramowicz, Jean-Jacques Legros, Alain Verloes, Michel Meurisse, Luc Van Gaal, Christine Verellen, Lucien Koulischer, Albert Beck

Journal:

Year:

1999

Language:

english

File:

PDF, 378 KB

english, 1999

12

Prenatal diagnosis of a dup(3p) with holoprosencephaly

Dr. Yves Gillerot, Jean Hustin, Lucien Koulischer, Vincent Viteux, Giovanni Neri, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 217 KB

english, 1987

13

Restrictive dermopathy

Dr. Yves Gillerot, Lucien Koulischer, Giovanni Neri

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 194 KB

english, 1987

14

Campomelic syndrome: Manifestations in a 20 week fetus and case history of a 5 year old child

Yves Gillerot, Claude-Annick Vanheck, Martine Foulon, Alain Podevain, Lucien Koulischer

Journal:

American Journal of Medical Genetics Part A

Year:

1989

Language:

english

File:

PDF, 429 KB

english, 1989

15

Mental retardation, short stature, almond-shaped eyes, small downturned mouth and coned epiphyses: A new case of Hunter-fraser syndrome

L. Van Maldergem, Y. Gillerot, N. Perlmutter, C. Wetzburger, L. Koulischer

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 295 KB

english, 1990

16

Etretinate embrytoxicity 7 months after discontinuation of treatment

Dr. Alain Verloes, Pol Dodinval, Lucien Koulischer, René Lambotte, Jacqueline Bonnivert

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 139 KB

english, 1990

17

Acromelic frontonasal “dysplasia”: Further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome)

Dr. Alain Verloes, Yves Gillerot, Elisabeth Walczak, Lionel Van Maldergem, Lucien Koulischer

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 388 KB

english, 1992

18

Restrictive dermopathy, a lethal form of arthrogryposis multiplex with skin and bone dysplasias: Three new cases and review of the literature

Dr. Alain Verloes, Nicole Mulliez, Marie Gonzales, Françoise Laloux, Trinh Hermanns-Lě, Gérald E. Piérard, Lucien Koulischer

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 976 KB

english, 1992

19

Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders: Review and delineation of the Cerebro-Acro-Visceral Early lethality (CAVE) multiplex syndrome

Dr. Alain Verloes, Yves Gillerot, Jean-Paul Langhendries, Jean-Pierre Fryns, Lucien Koulischer

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 1.11 MB

english, 1992

20

Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: A dominant disease with manifestations of Weill-Marchesani syndromes

Dr Alain Verloes, Jean-Paul Hermia, Albert Galand, Lucien Koulischer, Pol Dodinval

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 419 KB

english, 1992

21

New oral-acral syndrome with partial agenesis of the maxillary bones

Dr. Alain Verloes, Lucien Koulischer

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 257 KB

english, 1992

22

Pseudoaminopterin syndrome

Dr. Alain Verloes, Guy Bricteux, Lucien Koulischer

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 348 KB

english, 1993

23

Parkinsonian bradykinesia is due to depression in the rate of rise of muscle activity

Dr E. Godaux, D. Koulischer, J. Jacquy

Journal:

Annals of Neurology

Year:

1992

Language:

english

File:

PDF, 745 KB

english, 1992

24

Deletion of the 5′-ABL region: a recurrent anomaly detected by fluorescence in situ hybridization in about 10% of Philadelphia-positive chronic myeloid leukaemia patients

C. Herens, F. Tassin, V. Lemaire, Y. Beguin, E. Collard, S. Lampertz, C. Croisiau, M. Lecomte, B. De Prijk, L. Longrée, L. Koulischer

Journal:

British Journal of Haematology

Year:

2000

Language:

english

File:

PDF, 84 KB

english, 2000

25

Loss of the Y chromosome in bone marrow cells: results on 1907 consecutive cases of leukaemia and preleukaemia

C. Herens, E. Brasseur, M. Jamar, L. Vierset, I. Schoenen, L. Koulischer

Journal:

International Journal of Laboratory Hematology (Blackwell)

Year:

1999

Language:

english

File:

PDF, 137 KB

english, 1999

26

Non-radioactive assay of AFP, hCG, and uE3 from dried blood specimens: A low-cost alternative for maternal screening for trisomy 21

A. Verloes, R. Schoos, L. Koulischer

Journal:

Prenatal Diagnosis

Year:

1992

Language:

english

File:

PDF, 143 KB

english, 1992

27

Cytogenetic studies on wild house mice from Belgium

R. Hübner, L. Koulischer

Journal:

Year:

1990

Language:

english

File:

PDF, 479 KB

english, 1990

28

Down's syndrome in Wallonia (South Belgium), 1971–1978: Cytogenetics and incidence

L. Koulischer, Y. Gillerot

Journal:

Year:

1980

Language:

english

File:

PDF, 615 KB

english, 1980

29

Chromosome studies of a fertile mammalian hybrid: the offspring of the cross bongo × sitatunga (Bovoidea)

L. Koulischer, J. Tijskens, J. Mortelmans

Journal:

Year:

1973

Language:

english

File:

PDF, 689 KB

english, 1973

30

Lethal perinatal type II osteogenesis imperfecta in a family with a dominantly inherited type I

Y. Gillerot, J. M. Druart, L. Koulischer

Journal:

European Journal of Pediatrics

Year:

1983

Language:

english

File:

PDF, 1.08 MB

english, 1983

31

In vitro fertilization and embryo transfer at Loverval, Belgium

J. M. Debry, L. Koulischer

Journal:

Journal of Assisted Reproduction and Genetics

Year:

1988

Language:

english

File:

PDF, 187 KB

english, 1988

32

The Marshall-smith syndrome

A. Charon, Y. Gillerot, L. Van Maldergem, M. H. Van Schaftingen, B. de Bont, L. Koulischer

Journal:

European Journal of Pediatrics

Year:

1990

Language:

english

File:

PDF, 519 KB

english, 1990

33

Lethal short-rib with median cleft and without polydactyly: A fourth case

L. van Maldergem, Y. Gillerot, E. Salmin, A. Verloes, L. Koulischer

Journal:

Pediatric Radiology

Year:

1990

Language:

english

File:

PDF, 495 KB

english, 1990

34

Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test?

Verloes, Alain, Gillerot, Yves, Van Maldergem, Lionel, Schoos, Roland, Herens, Christian, Jamar, Mauricette, Dideberg, Vinciane, Lesenfants, Sylviane, Koulischer, Lucien

Journal:

European Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 75 KB

english, 2001

35

Etude clinique et cytogénétique de 21 patients atteints de leucémie myéloïde chronique

Y. Kenis, L. Koulischer

Journal:

European Journal of Cancer (1965)

Year:

1965

File:

PDF, 1.26 MB

1965

36

Mitotic chromatid separation in a case of acute leukemia

Journal:

European Journal of Cancer (1965)

Year:

1965

Language:

english

File:

PDF, 1.27 MB

english, 1965

37

Observations cytogénétiques dans la maladie de Vaquez

L. Koulischer, J. Frühling, J. Henry

Journal:

European Journal of Cancer (1965)

Year:

1965

File:

PDF, 2.48 MB

1965

38

Nuclear lesions during rat hepatocarcinogenesis

C. Herens, S. Massart, B. Bouzahzah, L. Koulischer, H. Barbason

Journal:

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

Year:

1995

Language:

english

File:

PDF, 824 KB

english, 1995

39

Nuclear lesions during rat hepatocarcinogenesis

C. Herens, M. Jacquemart, L. Koulischer, H. Barbason

Journal:

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

Year:

1995

Language:

english

File:

PDF, 661 KB

english, 1995

40

X-linked traits. A catalog of loci in non-human mammals: J. R. Miller. Cambridge University Press, New York. 1990. 198 pp. ISBN code 0-521-37389-1. Price $39.50

Journal:

Biochemical Systematics and Ecology

Year:

1992

Language:

english

File:

PDF, 76 KB

english, 1992

41

32 Review of 100 cases considered like MDS by clinicians

F. Tassin, J-P. Hermanne, C. Herens, L. Koulischer, N. Schaaf-Lafontaine, G. Fillet, J-M. Paulus

Journal:

Leukemia Research

Year:

1997

Language:

english

File:

PDF, 139 KB

english, 1997

42

Translocation (2;3)(p21;q26) as the Sole Anomaly in a Case of Primary Myelofibrosis

Christian Herens, Jean-Philippe Hermanne, Francoise Tassin, Marie France Fassotte, Albert Thiry, Mauricette Jamar, Nicole Schaaf-Lafontaine, Georges Fillet, Lucien Koulischer

Journal:

Cancer Genetics and Cytogenetics

Year:

1999

Language:

english

File:

PDF, 898 KB

english, 1999

43

Inv(12)(q15q24): A Nonrandom Change Associated with Myelodysplasia?

G Scantamburlo, S Lampertz, C Croisiau, M Jamar, L Koulischer, C Herens

Journal:

Cancer Genetics and Cytogenetics

Year:

2000

Language:

english

File:

PDF, 376 KB

english, 2000

44

Oro-facial-digital syndrome II

Yves Gillerot, Lucien Koulischer

Journal:

Clinical Genetics

Year:

1988

Language:

english

File:

PDF, 172 KB

english, 1988

45

Neural tube defects and omphalocele in trisomy 18

L. van Maldergem, Y. Gillerot, L. Koulischer

Journal:

Clinical Genetics

Year:

1989

Language:

english

File:

PDF, 206 KB

english, 1989

46

Primordial osteodysplastic dwarfism type I in association with corneal clouding: evidence for autosomal recessive inheritance

L. van Maldergem, Y. Gillerot, M. Godhaird, E. Nemec, L. Koulischer

Journal:

Clinical Genetics

Year:

1990

Language:

english

File:

PDF, 264 KB

english, 1990

47

Clinical overlap of Beckwith-Wiedemann, Perlman and Simpson-Golabi-Behmel syndromes: a diagnostic pitfall

Alan Verloes, Brigitte Massart, Isabelle Dehalleux, Jean-Paul Langhendries, Lucien Koulischer

Journal:

Clinical Genetics

Year:

1995

Language:

english

File:

PDF, 2.13 MB

english, 1995

48

A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondyly

Alain Verloes, Paul Jamblin, Lucien Koulischer, Jean-Pierre Bourguignon

Journal:

Clinical Genetics

Year:

1996

Language:

english

File:

PDF, 925 KB

english, 1996

49

L'isolation des cellules fœtales en circulation dans le sang maternel: mise au point

L Koulischer, C Herens, A Verloes, S Lesenfants

Journal:

Immuno-analyse & Biologie Spécialisée

Year:

1997

File:

PDF, 476 KB

1997

50

Cytogenetic study of bovine oocytes matured in vitro

F.J. Ectors, L. Koulischer, M. Jamar, C. Herens, A. Verloes, B. Remy, J-F. Beckers

Journal:

Year:

1995

Language:

english

File:

PDF, 640 KB

english, 1995

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