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1

Speciation and supersaturation model in papermaking streams

S. Clément, A. Gouiller, P. Ottenio, S. Nivelon, P. Huber, P. Nortier

Journal:

Process Safety and Environmental Protection

Year:

2011

Language:

english

File:

PDF, 525 KB

english, 2011

2

Interet de l'etude des vitesses de conduction nerveuse sensitive a l'aiguille chez l'enfant au-dessous de 3 ans

D. Audry-Chaboud, P. Soichot, M. Giroud, J.L. Nivelon

Journal:

Revue d'Electroencéphalographie et de Neurophysiologie Clinique

Year:

1984

File:

PDF, 231 KB

1984

3

Familial orofaciodigital syndrome type I revealed by ultrasound prenatal diagnosis of porencephaly

Christel Thauvin-Robinet, Thierry Rousseau, Christine Durand, Nicole Laurent, Catherine Maingueneau, Laurence Faivre, Paul Sagot, Annie Nivelon-Chevallier

Journal:

Prenatal Diagnosis

Year:

2001

Language:

english

File:

PDF, 130 KB

english, 2001

4

Alterations of Serum High-Density Lipoproteins and Hepatic Lipase Activity in Congenital Hypothyroidism

Tenenbaum, Denis, Gambert, Philippe, Fischbach, Michel, d’Athis, Philippe, Nivelon, Jean-Louis, Lallemant, Christian

Journal:

Year:

1988

File:

PDF, 1.67 MB

1988

5

STUDY OF FINAL HEIGHT IN TURNER SYNDROME(N = 216)

Rochiccioli, P, Battin, J, Bertrand, A M, Bouquier, J J, Bost, M, Chatelain, P, Colle, M, David, M, Freycon, R, Limal, J M, Malpuech, G, Mariani, R, Nivelon, J L, Pieron, M, Simonin, G, Sultan, C

Journal:

Pediatric Research

Year:

1993

Language:

english

File:

PDF, 140 KB

english, 1993

6

Dépistage de l'hyperplasie congénitale des surrénales par déficit en 21 hydroxylase (HSC)

Journal:

Archives de Pédiatrie

Year:

1995

File:

PDF, 152 KB

1995

7

Study of final height in Turner's syndrome: ethnic and genetic influences

Rochiccioli (Toulouse), P, David (Lyon), M, Malpuech (Clermont Ferrand), G, Colle (Bordeaux), M, Limal (Angers), J M, Battin (Bordeaux), J, Mariani (Nice), R, Sultan (Montpellier), C, Nivelon (Dijon),

Journal:

Acta Paediatrica

Year:

1994

Language:

english

File:

PDF, 364 KB

english, 1994

8

Effect of Preventive Phenobarbital Treatment on the Duration of Phototherapy in Low Birth Weight Icteric Twins

Gouyon, J.B., Collin, A., dâAthis, P., Dumas, M., Escousse, A., Couillault, G., Nivelon, J.L., Alison, M.

Journal:

Developmental Pharmacology and Therapeutics

Year:

1984

File:

PDF, 319 KB

1984

9

LETTER TO THE EDITOR. DE NOVO INTERSTITIAL PROXIMAL DELETION OF 14q AND PRENATAL DIAGNOSIS OF HOLOPROSENCEPHALY

H. BRUYERE, B. FAVRE, S. DOUVIER, A. NIVELON-CHEVALIER, F. MUGNERET

Journal:

Prenatal Diagnosis

Year:

1996

Language:

english

File:

PDF, 372 KB

english, 1996

10

A case of progressive familial encephalopathy in infancy with calcification of the basal ganglia and chronic cerebrospinal fluid lymphocytosis

M. Giroud, J. B. Gouyon, F. Chaumet, A. M. Cinquin, A. Chevalier-Nivelon, M. Alison, R. Dumas

Journal:

Child's Nervous System

Year:

1986

Language:

english

File:

PDF, 324 KB

english, 1986

11

Percentage of free serum prostate-specific antigen: A new tool in the early diagnosis of prostatic cancer

M.-E. Toubert, J. Guillet, M. Chiron, P. Meria, C. Role, M.-H. Schlageter, H. Francois, C. Borschneck, F. Nivelon, F. Desgrandchamps, D. Rastel, O. Cussenot, P. Teillac, A. Le Duc, Y. Najean

Journal:

European Journal of Cancer

Year:

1996

Language:

english

File:

PDF, 658 KB

english, 1996

12

Association of Marfan's Syndrome and Turner's Syndrome

Thauvin-Robinet, C., De Monleon, J.V., Nivelon-Chevallier, A., Petit, A., Huet, F.

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2001

Language:

english

File:

PDF, 872 KB

english, 2001

13

Hypocalcémie et hypomagnésé nie sévères secondaires à l'association d'une hypoparathy-roïdie et d'une tubulopathie hypokaliémique congénitale

F. Hdei, C. Mousson, G. Couillault, J.L. Nivelon

Journal:

Archives de Pédiatrie

Year:

1995

File:

PDF, 116 KB

1995

14

Investigation of a specific IgM antibody test in neonatal congenital syphilis.

Sepetjian, M, Tissot Guerraz, F, Monier, J C, Nivelon, J L, Thivolet, J

Journal:

Sexually Transmitted Infections

Year:

1970

Language:

english

File:

PDF, 365 KB

english, 1970

15

New autosomal recessive chondrodysplasia???pseudohermaphrodism syndrome

NIVELON, A., NIVELON, J-L., MABILLE, J-P., MAROTEAUX, P., FELDMAN, J-P., DOUVIER, S., AYM??, S.

Journal:

Clinical Dysmorphology

Year:

1992

File:

PDF, 2.86 MB

1992

16

AIP Conference Proceedings [Author(s) SOLARPACES 2015: International Conference on Concentrating Solar Power and Chemical Energy Systems - Cape Town, South Africa (13–16 October 2015)] - Second test campaign of a pilot scale latent heat thermal energy storage – Durability and operational strategies

Garcia, Pierre, Rougé, Sylvie, Nivelon, Pierre

Year:

2016

Language:

english

File:

PDF, 3.73 MB

english, 2016

17

Coffin-Lowry syndrome: a multicenter study

S. Gilgenkrantz, P. Mujica, P. Gruet, P. Tridon, F. Schweitzer, A. Nivelon-Chevallier, J. L. Nivelon, G. Couillault, A. David, A. Verloes, C. Lambotte, Ch. Piussan, M. Mathieu

Journal:

Clinical Genetics

Year:

1988

Language:

english

File:

PDF, 1.91 MB

english, 1988

18

Conservative management of cerebellar hematomas in neonates

J.B. Gouyon, M. Alison, J-L. Nivelon

Journal:

The Journal of Pediatrics

Year:

1981

Language:

english

File:

PDF, 169 KB

english, 1981

19

Serum Lipoproteins in Venous Blood Serum from Birth to the End of the First Week: Feeding Influences

Tenenbaum, Denis, Gambert, Philippe, Meunier, Sylvie, D’Athis, Philippe, Nivelon, Jean Louis, Lallemand, Christian

Journal:

Year:

1988

File:

PDF, 579 KB

1988

20

Vitamin K deficiency embryopathy

Van Kien, Philippe Khau, Nivelon-Chevallier, Annie, Spagnolo, Gilles, Douvier, Serge, Maingueneau, Catherine

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 166 KB

english, 1998

21

Probable localisation of the Coffin-Lowry locus in Xp22.2-P22.1 by multipoint linkage analysis

A. Hanauer, Y. Alembik, S. Gilgenkrantz, P. Mujica, A. Nivelon-Chevallier, M. E. Pembrey, I. D. Young, J. L. Mandel

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 349 KB

english, 1988

22

TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessment

Marie Gomot, Nathalie Ronce, Sabine Dessay, Ramzi Zemni, Anne-Dominique Ayrault, Marie-Pierre Moizard, Annie Nivelon, Simone Gilgenkrantz, Julliette Dourlens, Vincent Des Portes, Jamel Chelly, Claude

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 96 KB

english, 2002

23

A gene for blepharophimosis-ptosis-epicanthus inversus syndrome maps to chromosome 3q23

Patrizia Amati, Jean-Claude Chomel, Annie Nivelon-Chevalier, Simone Gilgenkrantz, Alain Kitzis, Josseline Kaplan, Dominique Bonneau

Journal:

Year:

1995

Language:

english

File:

PDF, 298 KB

english, 1995

24

Lipodystrophie de berardinelli diagnostic précoce chez un enfant portugais de parents consanguins

A Nivelon-Chevallier, C François, F Huet, J.L. Nivelon

Journal:

Archives de Pédiatrie

Year:

1997

File:

PDF, 108 KB

1997

25

A major locus for several phenotypes of myoclonus-dystonia on chromosome 7q

Vidailhet, M., Tassin, J., Durif, F., Nivelon-Chevallier, A., Agid, Y., Brice, A., Durr, A.

Journal:

Year:

2001

Language:

english

File:

PDF, 131 KB

english, 2001

26

Cerebrovascular disease in children under 16 years of age in the city of Dijon, France: A study of incidence and clinical features from 1985 to 1993

Maurice Giroud, Martine Lemesle, Jean-Bernard Gouyon, Jean-Louis Nivelon, Chantal Milan, Raymond Dumas

Journal:

Journal of Clinical Epidemiology

Year:

1995

Language:

english

File:

PDF, 625 KB

english, 1995

27

Le syndrome de smith lemli opitz Trois cas féminins de diagnostic néonatal. Difficultés de distinction entre les deux types

A Nivelon-Chevallier, C François, D Semama

Journal:

Archives de Pédiatrie

Year:

1997

File:

PDF, 108 KB

1997

28

Prenatal diagnosis of a partial trisomy 7q in two fetuses with bilateral ventriculomegaly

Christel Robinet, Serge Douvier, Philippe Khau Van Kien, Bernardine Favre, Isabelle Luquet, Nathalie Nadal, Annie Nivelon-Chevallier, Francine Mugneret

Journal:

Prenatal Diagnosis

Year:

2000

Language:

english

File:

PDF, 44 KB

english, 2000

29

Can Hutchinson-Gilford progeria syndrome be a neonatal condition?

Faivre, L., Van Kien, Ph. Khau, Madinier-Chappat, N., Nivelon-Chevallier, A., Beer, F., LeMerrer, M.

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 200 KB

english, 1999

30

Increased paternal age in CHARGE association

A.L. Tellier, S. Lyonnet, V. Cormier-Daire, P. de Lonlay, V. Abadie, C. Baumann, D. Bonneau, Ph. Labrune, D. Lacombe, M. Le Merrer, A. Nivelon, N. Philip, M. L. Briard, A. Munnich

Journal:

Clinical Genetics

Year:

1996

Language:

english

File:

PDF, 221 KB

english, 1996

31

Coupling a Chemical Reaction Engine with a Mass Flow Balance Process Simulation for Scaling Management in Papermaking Process Waters

Huber, Patrick, Nivelon, Sylvie, Ottenio, Pascal, Nortier, Patrice

Journal:

Industrial & Engineering Chemistry Research

Year:

2012

Language:

english

File:

PDF, 1.78 MB

english, 2012

32

Hypomandibular faciocranial dysostosis in consanguineous parents revealed by ultrasound prenatal diagnosis

Christel Thauvin-Robinet, Thierry Rousseau, Nicole Laurent, Christine Durand, Catherine Maingueneau, Valérie Cormier-Daire, Paul Sagot, Laurence Faivre, Annie Nivelon-Chevallier

Journal:

Prenatal Diagnosis

Year:

2002

Language:

english

File:

PDF, 176 KB

english, 2002

33

Aérosolthérapie et mucoviscidose: Enquête nationale

F. Huet, JL. Nivelon

Journal:

Archives de Pédiatrie

Year:

1996

File:

PDF, 117 KB

1996

34

A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene

Vincent, Christophe, Kalatzis, Vasiliki, Compain, Sylvie, Levilliers, Jacqueline, Slim, Rima, Graia, Fatima, Pereira, Maria de Lurdes, Nivelon, Annie, Croquette, Marie-France, Lacombe, Didier, Vignero

Journal:

Human Molecular Genetics

Year:

1994

Language:

english

File:

PDF, 1.64 MB

english, 1994

35

Late thalamic atrophy in infarction of the middle cerebral artery territory in neonates

Maurice Giroud, Hervé Fayolle, Didier Martin, Nathalie Baudoin, Nathalie André, Jean Bernard Gouyon, Jean Louis Nivelon, Raymond Dumas

Journal:

Child's Nervous System

Year:

1995

Language:

english

File:

PDF, 698 KB

english, 1995

36

Rattrapage statural des enfants ayant un déficit en hormone de croissance traités dès la première année de vie

F Huet, JC Carel, JL Nivelon, JL Chaussain

Journal:

Archives de Pédiatrie

Year:

1998

File:

PDF, 296 KB

1998

37

Unique survival in chrondrodysplasia-hermaphrodism syndrome

Christel Thauvin-Robinet, Francine Mugneret, Patrick Callier, Mondher Chouchane, Emmanuel Garron, Eric Manceau, Nicole Laurent, Christine Durand, Annie Nivelon-Chevallier, Emmanuel Sapin, Frédéric Hue

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 201 KB

english, 2005

38

Les méningites purulentes néo-natales à Moraxella glucidolytica (Bacterium anitratum)

Bernheim, M., Germain, D., Courtieu, A.-L., Nivelon, J.-L.

Journal:

Year:

1959

Language:

french

File:

PDF, 967 KB

french, 1959

39

Mazabraud syndrome in two patients: Clinical overlap with McCune-Albright syndrome

L. Faivre, A. Nivelon-Chevallier, M.L. Kottler, C. Robinet, P. Khau Van Kien, B. Lorcerie, A. Munnich, P. Maroteaux, V. Cormier-Daire, Dr. M. LeMerrer

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 128 KB

english, 2001

40

Hemiballismus revealing multiple sclerosis in an infant

M. Giroud, D. Semama, L. Pradeaux, J B. Gouyon, R. Dumas, J. L. Nivelon

Journal:

Child's Nervous System

Year:

1990

Language:

english

File:

PDF, 479 KB

english, 1990

41

Infantile systemic hyalinosis: a case with atypical prolonged survival

C Thauvin-Robinet, L Faivre, F Beer, E Justrabo, A Nivelon-Chevallier, F Huet

Journal:

Acta Paediatrica

Year:

2001

Language:

english

File:

PDF, 235 KB

english, 2001

42

Survey of LGMD2A mutations

I. Richard, L. Brenguier, B. Bady, M. Fardeau, C.A. Garcia, C.E. Jackson, D.M. Kurnit, G. Lefranc, C. Legums, J. Loiselet, L. Merlinil, A. Nivelon, E. Ollagnon, J.S. Beckmann

Journal:

Neuromuscular Disorders

Year:

1996

Language:

english

File:

PDF, 128 KB

english, 1996

43

Vitamin A deficiency and nocturnal vision in teenagers with cystic fibrosis

F. Huet, D. Semama, C. Maingueneau, A. Charavel, J.-L. Nivelon

Journal:

European Journal of Pediatrics

Year:

1997

Language:

english

File:

PDF, 134 KB

english, 1997

44

124 PRENATAL DIAGNOSIS OF 17-KETOSTEROID REDUCTASE DEFICIENCY

Forest, M G, Nivelon-Chevallier, A, Tenenbaum, P, Nivelon, J L

Journal:

Pediatric Research

Year:

1985

Language:

english

File:

PDF, 156 KB

english, 1985

45

Friedreich's ataxia: Point mutations and clinical presentation of compound heterozygotes

Mireille Cossée, Alexandra Dürr, Michèle Schmitt, Niklas Dahl, Paul Trouillas, Patricia Allinson, Markus Kostrzewa, Annie Nivelon-Chevallier, Karl-Henrik Gustavson, Alfried Kohlschütter, Ulrich Müller

Journal:

Annals of Neurology

Year:

1999

Language:

english

File:

PDF, 152 KB

english, 1999

46

Combined deficiency of β-galactosidase and neuraminidase: Three affected siblings in a French family

I. Maire, A. Nivelon-Chevallier

Journal:

Journal of Inherited Metabolic Disease

Year:

1981

Language:

english

File:

PDF, 226 KB

english, 1981

47

Exposure to hydroxyurea during pregnancy: a case series

Thauvin-Robinet, C, Maingueneau, C, Robert, E, Elefant, E, Guy, H, Caillot, D, Casasnovas, RO, Douvier, S, Nivelon-Chevallier, A

Journal:

Year:

2001

Language:

english

File:

PDF, 90 KB

english, 2001

48

Grippe et malformations congénitales

Bugnon, P., Mavel, A., Portier, H., Milan, C., Nivelon-Chevallier, A., Feldman, J.P., Michiels, Y.

Journal:

Médecine et Maladies Infectieuses

Year:

1980

Language:

french

File:

PDF, 1014 KB

french, 1980

49

PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY

Morel, Y, Murena, M, Forest, M G, Carel, J C, Leger, J, Nivelon, J-L, David, M

Journal:

Pediatric Research

Year:

1993

Language:

english

File:

PDF, 190 KB

english, 1993

50

Clinicopathological aspects of the neuropathy of neurogastrointestinal encephalomyopathy (MNGIE) in four patients including two with a Charcot–Marie–Tooth presentation

Gérard Said, Catherine Lacroix, Violaine Planté-Bordeneuve, Bernard Messing, Abdelhamid Slama, Pascal Crenn, Annie Nivelon-Chevallier, Laurent Bedenne, Pierre Soichot, E. Manceau, Daniel Rigaud, Anne

Journal:

Journal of Neurology

Year:

2005

Language:

english

File:

PDF, 459 KB

english, 2005

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