Results
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981.
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A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec. [electronic resource] by
- Merante, F
- Petrova-Benedict, R
- MacKay, N
- Mitchell, G
- Lambert, M
- Morin, C
- De Braekeleer, M
- Laframboise, R
- Gagné, R
- Robinson, B H
Producer: 19930809
In:
American journal of human genetics vol. 53
Availability: No items available.
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982.
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[Endomyocardial fibrosis: a rare case of restrictive cardiomyopathy in a Caucasian female]. [electronic resource] by
- Cuisset, T
- Nait Saidi, L
- Mouret, J P
- Barbou, F
- Quilici, J
- Fourcade, L
- Lambert, M
- Ghez, O
- Metras, D
- Bonnet, J L
Producer: 20060323
In:
Archives des maladies du coeur et des vaisseaux vol. 99
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983.
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984.
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985.
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Beta/A4-evoked degeneration of differentiated SH-SY5Y human neuroblastoma cells. [electronic resource] by
- Lambert, M P
- Stevens, G
- Sabo, S
- Barber, K
- Wang, G
- Wade, W
- Krafft, G
- Snyder, S
- Holzman, T F
- Klein, W L
Producer: 19950410
In:
Journal of neuroscience research vol. 39
Availability: No items available.
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986.
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[A case of losing one's head]. [electronic resource] by
- Fauchais, A L
- Ibaba, J
- Hachulla, E
- Delplace, J
- Michon-Pasturel, U
- Queyrel, V
- Lambert, M
- Hatron, P Y
- Cotten, A
- Devulder, B
Producer: 20020904
In:
La Revue de medecine interne vol. 23 Suppl 2
Availability: No items available.
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987.
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Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15. [electronic resource] by
- Debray, F-G
- Lambert, M
- Lemieux, B
- Soucy, J F
- Drouin, R
- Fenyves, D
- Dubé, J
- Maranda, B
- Laframboise, R
- Mitchell, G A
Producer: 20081231
In:
Journal of medical genetics vol. 45
Availability: No items available.
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988.
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Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies. [electronic resource] by
- Chelly, J
- Gilgenkrantz, H
- Lambert, M
- Hamard, G
- Chafey, P
- Récan, D
- Katz, P
- de la Chapelle, A
- Koenig, M
- Ginjaar, I B
Producer: 19910201
In:
Cell vol. 63
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989.
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990.
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Antiphospholipid antibodies in primary Sjögren's syndrome: prevalence and clinical significance in a series of 74 patients. [electronic resource] by
- Fauchais, A L
- Lambert, M
- Launay, D
- Michon-Pasturel, U
- Queyrel, V
- Nguyen, N
- Hebbar, M
- Hachulla, E
- Devulder, B
- Hatron, P Y
Producer: 20040819
In:
Lupus vol. 13
Availability: No items available.
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991.
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992.
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993.
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994.
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[Hypertrophic myopathy due to muscular metastasis of a signet cell adenocarcinoma of the bladder]. [electronic resource] by
- Brénuchon, C
- Launay, D
- Maurage, C A
- Queyrel, V
- Lambert, M
- N'Guyen, H D
- Boutry, N
- Hachulla, E
- Hatron, P Y
- Devulder, B
Producer: 20050215
In:
La Revue de medecine interne vol. 25
Availability: No items available.
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995.
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[Pseudo-adult Still's disease, anasarca, thrombotic thrombocytopenic purpura and dysautonomia: An atypical presentation of multicentric Castleman's disease. Discussion of TAFRO syndrome]. [electronic resource] by
- Jouvray, M
- Terriou, L
- Meignin, V
- Bouchindhomme, B
- Jourdain, M
- Lambert, M
- Lefevre, G
- Hachulla, E
- Hatron, P-Y
- Galicier, L
- Launay, D
Producer: 20161019
In:
La Revue de medecine interne vol. 37
Availability: No items available.
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996.
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Genetic epidemiology of lipoprotein lipase deficiency in Saguenay-Lac-St-Jean (Québec, Canada). [electronic resource] by
- Dionne, C
- Gagné, C
- Julien, P
- Murthy, M R
- Lambert, M
- Roederer, G
- Davignon, J
- Hayden, M R
- Lupien, P J
- de Braekeleer, M
Producer: 19921015
In:
Annales de genetique vol. 35
Availability: No items available.
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997.
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Expression of the transcripts initiated in the 62nd intron of the dystrophin gene. [electronic resource] by
- Lambert, M
- Chafey, P
- Hugnot, J P
- Koulakoff, A
- Berwald-Netter, Y
- Billard, C
- Morris, G E
- Kahn, A
- Kaplan, J C
- Gilgenkrantz, H
Producer: 19940623
In:
Neuromuscular disorders : NMD vol. 3
Availability: No items available.
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998.
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[Euthyroid Graves' disease: a case report]. [electronic resource] by
- Hornez, N
- Morell-Dubois, S
- Woillez, J-P
- Queyrel, V
- Charlanne, H
- Launay, D
- Lambert, M
- Hachulla, E
- Wemeau, J-L
- Hatron, P-Y
Producer: 20100202
In:
La Revue de medecine interne vol. 30
Availability: No items available.
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999.
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Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients. [electronic resource] by
- Lemay, J F
- Lambert, M A
- Mitchell, G A
- Vanasse, M
- Valle, D
- Arbour, J F
- Dubé, J
- Flessas, J
- Laberge, M
- Lafleur, L
Producer: 19921218
In:
The Journal of pediatrics vol. 121
Availability: No items available.
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1000.
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Structure of the catalytic domain of fibroblast collagenase complexed with an inhibitor. [electronic resource] by
- Lovejoy, B
- Cleasby, A
- Hassell, A M
- Longley, K
- Luther, M A
- Weigl, D
- McGeehan, G
- McElroy, A B
- Drewry, D
- Lambert, M H
Producer: 19940210
In:
Science (New York, N.Y.) vol. 263
Availability: No items available.
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