Results of search for 'au:"ROLLAND, M"' › مکتبة رقمیه للعلوم الطبيه catalog

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- 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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- Amino Acid Sequence
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- Infant, Newborn
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	181.	[Delayed diagnosis of homocystinuria by major deficiency in cystathionine beta synthase]. [electronic resource] by Tur, M-D De Maistre, E Franck, P Rolland, M-O Fremont, S Lecompte, T Vidailhet, M Producer: 20040309 In: La Revue de medecine interne vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	182.	Growth hormone, insulin-like growth factor-I and insulin-like growth factor binding protein-3 are regulated differently in small-for-gestational-age and appropriate-for-gestational-age neonates. [electronic resource] by Cance-Rouzaud, A Laborie, S Bieth, E Tricoire, J Rolland, M Grandjean, H Rochiccioli, P Tauber, M Producer: 19990112 In: Biology of the neonate vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	183.	Prenatal diagnosis of non-ketotic hyperglycinaemia: enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutations. [electronic resource] by Kure, S Rolland, M O Leisti, J Mandel, H Sakata, Y Tada, K Matsubara, Y Narisawa, K Producer: 19991109 In: Prenatal diagnosis vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	184.	[Follicular atrophoderma, basal cell proliferation and hypotrichosis (Bazex-Dupré-Christol syndrome). A study in 2 families]. [electronic resource] by Moreau-Cabarrot, A Bonafé, J L Hachich, N Jalby, B C Aubert, G Rolland, M Bazex, J Producer: 19950502 In: Annales de dermatologie et de venereologie vol. 121 Availability: No items available. Save to lists Add to cart (remove)
	185.	Non-concordance of CVS and liver glycine cleavage enzyme in three families with non-ketotic hyperglycinaemia (NKH) leading to false negative prenatal diagnoses. [electronic resource] by Applegarth, D A Toone, J R Rolland, M O Black, S H Yim, D K Bemis, G Producer: 20000630 In: Prenatal diagnosis vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	186.	[Late onset 3-HMG-CoA lyase deficiency: a rare but treatable disorder]. [electronic resource] by Pierron, S Giudicelli, H Moreigne, M Khalfi, A Touati, G Caruba, C Rolland, M-O Acquaviva, C Producer: 20100430 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	187.	Primary hyperoxaluria in infants: medical, ethical, and economic issues. [electronic resource] by Cochat, P Koch Nogueira, P C Mahmoud, M A Jamieson, N V Scheinman, J I Rolland, M O Producer: 19991230 In: The Journal of pediatrics vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	188.	[Late diagnosis of a McArdle disease's case (type V glycogenosis)]. [electronic resource] by Flavier, S Rolland, M O Eude, M Fédou, C Brun, J F Maire, I Mercier, J Raynaud, E Producer: 20071218 In: Annales de biologie clinique vol. 65 Availability: No items available. Save to lists Add to cart (remove)
	189.	[Neonatal detection of congenital hypothyroidism by TSH determination in dried blood stain. 2 years of experience]. [electronic resource] by David, M Dorche, C Rolland, M O Feit, J P Chopard, A Teyssier, G Cotte, J Jeune, M Producer: 19790816 In: La Nouvelle presse medicale vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	190.	Resistance to erucic acid as a selectable marker for peroxisomal activity: isolation of revertants of an infantile Refsum disease cell line. [electronic resource] by Bachir Bioukar, E Straehli, F Ng, K H Rolland, M O Hashimoto, T Carreau, J P Deschatrette, J Producer: 19940908 In: Journal of inherited metabolic disease vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	191.	Placental taurine and low birth weight infants. [electronic resource] by Ghisolfi, J Berrebi, A Nguyen, V B Thouvenot, J P Rolland, M Putet, G Dabadie, A Pontonnier, G Producer: 19891219 In: Biology of the neonate vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	192.	Fetal type IV glycogen storage disease: clinical, enzymatic, and genetic data of a pure muscular form with variable and early antenatal manifestations in the same family. [electronic resource] by L'herminé-Coulomb, A Beuzen, F Bouvier, R Rolland, M O Froissart, R Menez, F Audibert, F Labrune, P Producer: 20060424 In: American journal of medical genetics. Part A vol. 139A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	193.	[Maternofetal infection with human parvovirus B19. Apropos of 2 cases]. [electronic resource] by Bernard, J D Berrebi, A Sarramon, M F Bloom, M C Rolland, M Icart, J Morinet, F Fournie, A Producer: 19920901 In: Journal de gynecologie, obstetrique et biologie de la reproduction vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	194.	Localization of Refsum disease with increased pipecolic acidaemia to chromosome 10p by homozygosity mapping and carrier testing in a single nuclear family. [electronic resource] by Nadal, N Rolland, M O Tranchant, C Reutenauer, L Gyapay, G Warter, J M Mandel, J L Koenig, M Producer: 19960418 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	195.	[Severe hyperhomocysteinemia revealing homocystinuria in two young adults with mild phenotype]. [electronic resource] by Ducros, V Rousset, J Garambois, K Boujet, C Rolland, M O Valenti, K Bouillet, L Jaillard, A Favier, A Producer: 20060321 In: La Revue de medecine interne vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	196.	[Care and outcome of 55 children born to HIV seropositive mothers]. [electronic resource] by Tricoire, J Robert, A Berrebi, A Puel, J Rolland, M Gayet-Mengelle, C Herne, P Rousseau, A Regnier, C Producer: 19891017 In: Archives francaises de pediatrie vol. 46 Availability: No items available. Save to lists Add to cart (remove)
	197.	Partial deletion of the AGXT gene (EX1_EX7del): A new genotype in hyperoxaluria type 1. [electronic resource] by Nogueira, P K Vuong, T S Bouton, O Maillard, A Marchand, M Rolland, M O Cochat, P Bozon, D Producer: 20000428 In: Human mutation vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	198.	Inter-observer agreement of a comprehensive health status classification system for pre-school children among patients with Wilms' tumor or advanced neuroblastoma. [electronic resource] by Nathan, P C Furlong, W Horsman, J Van Schaik, C Rolland, M Weitzman, S Feeny, D Barr, R D Producer: 20050217 In: Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	199.	[Homocystinuria and chronic respiratory insufficiency. Apropos of a case]. [electronic resource] by Andlauer, A C David, M Feit, J P Macabeo, V Vibert, J Collombel, C Rolland, M O Jeune, M Producer: 19790428 In: Pediatrie vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	200.	Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus material. [electronic resource] by Kvittingen, E A Guibaud, P P Divry, P Mandon, G Rolland, M O Domenichini, Y Jakobs, C Christensen, E Producer: 19860718 In: European journal of pediatrics vol. 144 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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