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Results of search for 'au:"ROLLAND, M"', page 8 of 12
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Authors
Arnaud, C
Berrebi, A
Bloom, M C
Cotte, J
Divry, P
Guibaud, P
LISSITZKY, S
Lejeune, P J
Lissitzky, S
Marriq, C
Martinez, J
Mathieu, M
ROLLAND, M
Regnier, C
Rolland, M
Rolland, M O
Régnier, C
Sarramon, M F
THIVOLET, J
Tricoire, J
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Adult
Amino Acid Sequence
Animals
Child
Child, Preschool
Female
Humans
Infant
Infant, Newborn
Male
Pregnancy
Prenatal Diagnosis
Thyroglobulin
analysis
blood
chemistry
deficiency
diagnosis
genetics
metabolism
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Undetermined
Your search returned 237 results.
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141.
False-positive results in neonatal screening for cystic fibrosis based on a three-stage protocol (IRT/DNA/IRT): Should we adjust IRT cut-off to ethnic origin?
[electronic resource]
by
Cheillan, D
Vercherat, M
Chevalier-Porst, F
Charcosset, M
Rolland, M O
Dorche, C
Producer:
20060705
In:
Journal of inherited metabolic disease
vol. 28
Online resources:
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142.
[Pyridoxine-dependent convulsions : familial case].
[electronic resource]
by
Lauras, B
Drevon, B
Rolland, M O
Teyssier, G
Bovier-Lapierre, M
Freycon, F
Producer:
19841025
In:
Pediatrie
vol. 39
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143.
[Maternofetal infection by parvovirus associated with antenatal meconium peritonitis].
[electronic resource]
by
Bloom, M C
Rolland, M
Bernard, J D
Fournié, A
Berrebi, A
Régnier, C
Producer:
19901026
In:
Archives francaises de pediatrie
vol. 47
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144.
[Acute fetal distress: medium-term neurological prognosis].
[electronic resource]
by
Dupic, Y
Rolland, M
Mas, M F
Berges, J L
Monnier, L
Régnier, C
Producer:
19800712
In:
Pediatrie
vol. 34
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145.
A 13-bp deletion (1952 del 13) in the methylmalonyl CoA mutase gene of an affected patient.
[electronic resource]
by
Touraine, R L
Rolland, M O
Divry, P
Mathieu, M
Guibaud, P
Bozon, D
Producer:
19950906
In:
Human mutation
vol. 5
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146.
First-trimester prenatal diagnosis of Canavan disease.
[electronic resource]
by
Rolland, M O
Divry, P
Mandon, G
Thoulon, J M
Fiumara, A
Mathieu, M
Producer:
19950817
In:
Journal of inherited metabolic disease
vol. 16
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147.
Prenatal diagnosis of combined methylmalonic aciduria and homocystinuria (cobalamin CblC or CblD mutant)
[electronic resource]
by
Chadefaux-Vekemans, B
Rolland, M O
Lyonnet, S
Rabier, D
Divry, P
Kamoun, P
Producer:
19941010
In:
Prenatal diagnosis
vol. 14
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148.
A new case of 2-methylacetoacetyl-CoA thiolase deficiency?
[electronic resource]
by
Renom, G
Fontaine, M
Rolland, M O
Duprey, J
Degand, P M
Dobbelaere, D
Producer:
20010308
In:
Journal of inherited metabolic disease
vol. 23
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149.
Prenatal diagnosis of craniosynostosis: value of MR imaging.
[electronic resource]
by
Fjørtoft, M Irsutti
Sevely, A
Boetto, S
Kessler, S
Sarramon, M F
Rolland, M
Producer:
20071025
In:
Neuroradiology
vol. 49
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150.
[Predictive value of non-specific signs of fetal infection in congenital toxoplasmosis].
[electronic resource]
by
Berrebi, A
Cohen-Khallas, Y
Bessières, M H
Rolland, M
Sarramon, M F
Fournié, A
Producer:
19930127
In:
Journal de gynecologie, obstetrique et biologie de la reproduction
vol. 21
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151.
Regional assignment of the ADA locus on 20q13.2 leads to qter by gene dosage studies.
[electronic resource]
by
Philip, T
Lenoir, G
Rolland, M O
Philip, I
Hamet, M
Lauras, B
Fraisse, J
Producer:
19801024
In:
Cytogenetics and cell genetics
vol. 27
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152.
Antenatal detection of subdiaphragmatic pulmonary sequestration: a case report.
[electronic resource]
by
Baunin, C
Puget, C
Guitard, J
Rubie, H
Robert, A
Rolland, M
Sarramon, M F
Producer:
19941017
In:
European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie
vol. 4
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153.
[TSH, FT4 and T3T evaluation in normal and preterm hospitalized newborns].
[electronic resource]
by
Cartault Grandmottet, A
Cristini, C
Tricoire, J
Rolland, M
Tauber, M-T
Salles, J-P
Producer:
20070403
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 14
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154.
Taurine in developing brain, liver and muscle in infants.
[electronic resource]
by
Ghisolfi, J
Nguyen, V B
Thouvenot, J P
Rolland, M
Putet, G
Lapalu-Traon, C
Producer:
19891219
In:
Biology of the neonate
vol. 56
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155.
[Comparative study of radioimmunologic and immunoenzyme methods for the determination of alpha feto-protein].
[electronic resource]
by
Arnaud, C
Lejeune, P J
Blanc, J G
Rolland, M
Chagnon, C
Bernard, P J
Producer:
19840917
In:
Pathologie-biologie
vol. 32
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156.
Metabolic studies in twin brothers with 2-methylacetoacetyl-CoA thiolase deficiency.
[electronic resource]
by
Fontaine, M
Briand, G
Ser, N
Armelin, I
Rolland, M O
Degand, P
Vamecq, J
Producer:
19970305
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 255
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157.
Diagnostic value of serum immunoglobulinaemia D level in patients with a clinical suspicion of hyper IgD syndrome.
[electronic resource]
by
Ammouri, W
Cuisset, L
Rouaghe, S
Rolland, M-O
Delpech, M
Grateau, G
Ravet, N
Producer:
20081204
In:
Rheumatology (Oxford, England)
vol. 46
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158.
[Partial monosomy 20q : a new syndrome. Regional assignment of the ADA locus on 20q132 (author's transl)].
[electronic resource]
by
Fraisse, J
Bertheas, M F
Frère, F
Lauras, B
Rolland, M O
Brizard, C P
Producer:
19821021
In:
La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris
vol. 58
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159.
[Clouston's ectodermal dysplasia. A case report with biochemical study of keratin].
[electronic resource]
by
Giraud, F
Mattei, J F
Rolland, M
Ghiglione, C
Pommier de Sante, P
Sudan, N
Producer:
19780524
In:
Archives francaises de pediatrie
vol. 34
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160.
[Major aplasia of the thoracic wall and congenital thoracic scoliosis (3 observations) (author's transl)].
[electronic resource]
by
Gaubert, J
Régnier, C
Rochiccioli, P
Gaillard, J
Rolland, M
Bardier, M
Planques, L P
Producer:
19820212
In:
Chirurgie pediatrique
vol. 22
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