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1
Resolution of coronary arteritis following tuberculosis treatment
Resolution of coronary arteritis following tuberculosis treatment
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Resolution of coronary arteritis following tuberculosis treatment

Barreto-Neto, Nestor ; Segre, Alexandre W ; Guedes, Lissiane K N ; Seguro, Luciana P C ; Pereira, Rosa M R

Journal of clinical tuberculosis and other mycobacterial diseases, 2022, Vol.26, p.100295-100295

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2
Compensatory education for cultural deprivation, B. S. Bloom, A. Davis, R. Hess. 1965
Compensatory education for cultural deprivation, B. S. Bloom, A. Davis, R. Hess. 1965
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Compensatory education for cultural deprivation, B. S. Bloom, A. Davis, R. Hess. 1965

Segré, Monique

Revue française de pédagogie, 1967, Vol.1 (1), p.39-40

PERSÉE : Université de Lyon, CNRS & ENS de Lyon

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3
High Energy Alpha Particles Associated with Fission
High Energy Alpha Particles Associated with Fission
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High Energy Alpha Particles Associated with Fission

Wollan, E. O ; Moak, Charles D ; Sawyer, R. B

1947

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4
Deep pyoderma caused by Burkholderia cepacia complex associated with ciclosporin administration in dogs: a case series
Deep pyoderma caused by Burkholderia cepacia complex associated with ciclosporin administration in dogs: a case series
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Deep pyoderma caused by Burkholderia cepacia complex associated with ciclosporin administration in dogs: a case series

Banovic, Frane ; Koch, Sandra ; Robson, David ; Jacob, Megan ; Olivry, Thierry

Veterinary Dermatology, 2015, Vol.26 (4), p.287-e64

Blackwell Publishing Ltd

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5
Cervical tumoral calcinosis with secondary hyperparathyroidism in a chronic hemodialysis patient
Cervical tumoral calcinosis with secondary hyperparathyroidism in a chronic hemodialysis patient
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Cervical tumoral calcinosis with secondary hyperparathyroidism in a chronic hemodialysis patient

Sunder, Sham ; Verma, Himanshu ; Venkataramanan, Krishnamoorthy

Hemodialysis International, 2013, Vol.17 (3), p.458-462

Blackwell Publishing Ltd

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6
A 10.46 Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism
A 10.46 Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism
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A 10.46 Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism

Soysal, Yasemin ; Vermeesch, Joris ; Davani, Nooshin Ardeshir ; Hekimler, Kuyaş ; İmirzalıoğlu, Necat

American Journal of Medical Genetics Part A, 2011, Vol.155A (7), p.1745-1752

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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7
Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters
Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters
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Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters

Harrison, Victoria ; Connell, Lyndsey ; Hayesmoore, Jesse ; McParland, Joanna ; Pike, Michael G. ; Blair, Edward

American Journal of Medical Genetics Part A, 2011, Vol.155A (11), p.2826-2831

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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8
Mosaic partial trisomy 19p12-q13.11 due to a small supernumerary marker chromosome: A locus associated with Asperger syndrome?
Mosaic partial trisomy 19p12-q13.11 due to a small supernumerary marker chromosome: A locus associated with Asperger syndrome?
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Mosaic partial trisomy 19p12-q13.11 due to a small supernumerary marker chromosome: A locus associated with Asperger syndrome?

Faucz, Fabio Rueda ; Souza, Josiane ; Filho, Aguinaldo Bonalumi ; Sotomaior, Vanessa Santos ; Frantz, Egon ; Antoniuk, Sergio ; Rosenfeld, Jill A. ; Raskin, Salmo

American Journal of Medical Genetics Part A, 2011, Vol.155A (9), p.2308-2310

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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9
A case of autism with an interstitial 1q deletion (1q23.3-24.2) and a de novo translocation of chromosomes 1q and 5q
A case of autism with an interstitial 1q deletion (1q23.3-24.2) and a de novo translocation of chromosomes 1q and 5q
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A case of autism with an interstitial 1q deletion (1q23.3-24.2) and a de novo translocation of chromosomes 1q and 5q

Della Monica, Matteo ; Lonardo, Fortunato ; Faravelli, Francesca ; Pierluigi, Mauro ; Luquetti, Daniela Varela ; De Gregori, Manuela ; Zuffardi, Orsetta ; Scarano, Gioacchino

American Journal of Medical Genetics Part A, 2007, Vol.143A (22), p.2733-2737

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
Fanconi's Syndrome in a Dog With Primary Hypoparathyroidism
Fanconi's Syndrome in a Dog With Primary Hypoparathyroidism
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Fanconi's Syndrome in a Dog With Primary Hypoparathyroidism

Freeman, Lisa M. ; Breitschwerdt, Edward B. ; Keene, Bruce W. ; Hansen, Bernie

Journal of Veterinary Internal Medicine, 1994, Vol.8 (5), p.349-354

Oxford, UK: Blackwell Publishing Ltd

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