S Sanjad: search on Z-Library

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1

A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.

S. A. Sanjad, N. A. Sakati, Y. K. Abu-osba, R. Kaddoura, R. D. Milner

Year:

1991

Language:

english

File:

PDF, 1.15 MB

english, 1991

2

Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK

Simon, David B., Karet, Fiona E., Rodriguez-Soriano, Juan, Hamdan, Jahed H., DiPietro, Antonio, Trachtman, Howard, Sanjad, Sami A., Lifton, Richard P.

Journal:

Nature Genetics

Year:

1996

File:

PDF, 536 KB

1996

3

Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing (rdRTA2) to 7q33-34

Fiona E. Karet, Karin E. Finberg, Ahmet Nayir, Aysin Bakkaloglu, Seza Ozen, Sally A. Hulton, Sami A. Sanjad, Essam A. Al-Sabban, Juan F. Medina, Richard P. Lifton

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 2.03 MB

english, 1999

4

Congenital nephrotic syndrome and nonsteroidal anti-inflammatory drugs

Aoun, B, Ulinski, T, Kalkas, G, Schmitt, CP, Fakhoury, H, Sanjad, S

Journal:

Indian Journal of Nephrology

Year:

2012

Language:

english

File:

PDF, 473 KB

english, 2012

5

Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets

Hanna, A.E., Sanjad, S., Andary, R., Nemer, G., Ghafari, J.G.

Journal:

JDR Clinical & Translational Research

Year:

2018

Language:

english

File:

PDF, 418 KB

english, 2018

6

Should pediatric kidneys be used in cadaveric kidney transplantation?

K Alshaibani, S Raza, K Almeshari, O Alfurayh, I Alahmadi, E Alsabban, S Sanjad

Journal:

Transplantation Proceedings

Year:

1998

Language:

english

File:

PDF, 124 KB

english, 1998

7

A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity

B. Burwinkel,S.A. Sanjad,E. Al-Sabban,A. Al-Abbad,M.W. Kilimann

Journal:

Year:

1999

Language:

english

File:

PDF, 77 KB

english, 1999

8

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

Choi, M., Scholl, U. I., Ji, W., Liu, T., Tikhonova, I. R., Zumbo, P., Nayir, A., Bakkaloglu, A., Ozen, S., Sanjad, S., Nelson-Williams, C., Farhi, A., Mane, S., Lifton, R. P.

Journal:

Proceedings of the National Academy of Sciences

Year:

2009

Language:

english

File:

PDF, 1.05 MB

english, 2009

9

Acute Glomerulonephritis in Children

SANJAD, SAMI, TOLAYMAT, ASAD, Y, J A, LEVIN, SIDNEY

Journal:

Southern Medical Journal

Year:

1977

File:

PDF, 447 KB

1977

10

1201 Whole Exon Deletion in the Claudin 16 Gene, a Novel Mutation in Familial Hypomagnesemia/Hypercalciuria/Nephrocalcinosis (FHHNC) and Sensorineural Deafness (SND)

Sanjad, S., Lu, Y., Khoury, C., Habbal, Z., Lifton, R.

Journal:

Archives of Disease in Childhood

Year:

2012

Language:

english

File:

PDF, 618 KB

english, 2012

11

Documentos para a história do mais antigo jardim zoológico do Brasil: o parque zoobotânico do Museu Goeldi

Sanjad, Nelson, Oren, David Conway, Silva Junior, José de Sousa e, Hoogmoed, Marinus Steven, Higuchi, Horácio

Journal:

Boletim do Museu Paraense Emílio Goeldi Ciências Humanas

Year:

2012

File:

PDF, 2.18 MB

2012

12

Cólera e medicina ambiental no manuscrito 'Cholera-morbus' (1832), de Antonio Correa de Lacerda (1777-1852)

Journal:

História, Ciências, Saúde-Manguinhos

Year:

2004

File:

PDF, 239 KB

2004

13

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na–K–2CI cotransporter NKCC2

Simon, David B., Karet, Fiona E., Hamdan, Jahed M., Pietro, Antonio Di, Sanjad, Sami A., Lifton, Richard P.

Journal:

Nature Genetics

Year:

1996

File:

PDF, 920 KB

1996

14

University of Wisconsin versus eurocollins solution for kidney preservation: analysis of clinical outcome

K Alshaibani, N Nizamuddin, S Raza, O Alfurayh, K Almeshari, W Qunibi, E Sanjad

Journal:

Transplantation Proceedings

Year:

1998

Language:

english

File:

PDF, 122 KB

english, 1998

15

Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency

E Al-Jishi, Bf Meyer, Ms Rashed, M Al-Essa, Mh Al-Hamed, N Sakati, S Sanjad, Pt Ozand, M Kambouris

Journal:

Clinical Genetics

Year:

1999

Language:

english

File:

PDF, 266 KB

english, 1999

16

Chronic Peritoneal Dialysis in Lebanese Children of Families with Low Socioeconomic Status

Aoun, B., Ulinski, T., Sanjad, S., Termos, S., Dahrouj, M., Fakhoury, H., Schmitt, C. P.

Journal:

Peritoneal Dialysis International

Year:

2015

Language:

english

File:

PDF, 813 KB

english, 2015

17

Norovirus: a novel etiologic agent in hemolytic uremic syndrome in an infant

Abu Daher, Ghadi, Aoun, Bilal, Jaafar, Fatima, Khafaja, Sarah, Sanjad, Sami

Journal:

Year:

2019

Language:

english

File:

PDF, 659 KB

english, 2019

18

Pamidronate Rescue Therapy for Hypercalcemia in a Child With Williams Syndrome

Sanjad, Sami A., Aoun, Bilal, Yammine, Halim, Bassyouni, Amina, Karam, Pascale E.

Journal:

Frontiers in Endocrinology

Year:

2018

Language:

english

File:

PDF, 119 KB

english, 2018

19

Da 'abominável profissão de vampiros': Emílio Goeldi e Os mosquitos no Pará (1905)

Journal:

História, Ciências, Saúde-Manguinhos

Year:

2003

File:

PDF, 1.45 MB

2003

20

Norovirus: a novel etiologic agent in hemolytic uremic syndrome in an infant

Abu Daher, Ghadi, Aoun, Bilal, Jaafar, Fatima, Khafaja, Sarah, Sanjad, Sami

Journal:

Year:

2019

File:

PDF, 659 KB

2019

21

Management of hyperlipidemia in children with refractory nephrotic syndrome: The effect of statin therapy

Sami A. Sanjad, Abbas Al-Abbad, Saleh Al-Shorafa

Journal:

The Journal of Pediatrics

Year:

1997

Language:

english

File:

PDF, 482 KB

english, 1997

22

Intensive care and immediate follow-up of children after renal transplantation

M.G Seikaly, S.A Sanjad

Journal:

Transplantation Proceedings

Year:

2001

Language:

english

File:

PDF, 77 KB

english, 2001

23

Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes

Andary, Rabih, El-Hage-Sleiman, Abdul-Karim, Farhat, Theresa, Sanjad, Sami, Nemer, Georges

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2017

Language:

english

File:

PDF, 2.65 MB

english, 2017

24

Exposições internacionais: uma abordagem historiográfica a partir da América Latina

Journal:

História, Ciências, Saúde-Manguinhos

Year:

2017

Language:

english

File:

PDF, 319 KB

english, 2017

25

Childhood acute leukemia: A search for occult extramedullary disease prior to discontinuation of chemotherapy

D. H. Mahoney Jr., E. T. Gonzales, G. D. Ferry, S. A. Sanjad, G. K. Von Noorden, D. J. Fernbach

Journal:

Year:

1981

Language:

english

File:

PDF, 315 KB

english, 1981

26

Fanconi's Syndrome With Hepatorenal Glycogenosis Associated With Phosphorylase b Kinase Deficiency

Sanjad, Sami A.

Journal:

Archives of Pediatrics and Adolescent Medicine

Year:

1993

Language:

english

File:

PDF, 1.74 MB

english, 1993

27

Renal Hypoprostaglandism, Hypertension, and Type IV Renal Tubular Acidosis Reversed by Furosemide

SANJAD, SAMI A.

Journal:

Annals of Internal Medicine

Year:

1983

Language:

english

File:

PDF, 806 KB

english, 1983

28

Distinctive vasculopathy with systemic involvement due to levamisole long-term therapy: a case report

Aoun, Bilal, Alali, Mohammad, Degheili, Jad A., Sanjad, Sami, Vaquin, Claudine, Donadieu, Jean, Ulinski, Tim, Termos, Salah

Journal:

Journal of Medical Case Reports

Year:

2018

Language:

english

File:

PDF, 1.49 MB

english, 2018

29

Comércio, política e ciência nas exposições internacionais. O Brasil em Turim, 1911. Parte 1

Sanjad, Nelson, Castro, Anna Raquel de Matos

Journal:

Year:

2015

File:

PDF, 1.03 MB

2015

30

Nephropathy, an underestimated complication of methicillin therapy

William L. Nyhan, Sami A. Sanjad, Gabriel G. Haddad, Victor H. Nassar

Journal:

The Journal of Pediatrics

Year:

1974

Language:

english

File:

PDF, 1.17 MB

english, 1974

31

The historical glazed tiles from Nossa Senhora da Soledade Cemetery, Northern Brazil: microstructural, physical and mineralogical characterization

Gasparetto, S. A. M., Sanjad, T. A. B. C.

Journal:

Year:

2018

File:

PDF, 2.23 MB

2018

32

Bartter syndrome in a neonate: early treatment with indomethacin

C. C. Mourani, S. A. Sanjad, C. Y. Akatcherian

Journal:

Pediatric Nephrology

Year:

2000

Language:

english

File:

PDF, 89 KB

english, 2000

33

Renal tubular dysfunction following kidney transplantation: a prospective study in 31 children

S.A Sanjad, A Ibrahim, S Al Shorafa, A Al Abbad, R.B Khauli, K.A.P Shaibani, E Al Sabban

Journal:

Transplantation Proceedings

Year:

2001

Language:

english

File:

PDF, 60 KB

english, 2001

34

A novelPCLN-1gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype

Sami A. Sanjad, Ali Hariri, Zouhayr M. Habbal, Richard P. Lifton

Journal:

Pediatric Nephrology

Year:

2007

Language:

english

File:

PDF, 183 KB

english, 2007

35

The kidney transplant program at king faisal specialist hospital and research center: results of the last 10 years

K Alshaibani, S Raza, O Alfurayh, K Almeshari, W Qunibi, I Alahmadi, E Alsabban, S Sanjad

Journal:

Transplantation Proceedings

Year:

1998

Language:

english

File:

PDF, 610 KB

english, 1998

36

The metal alloys from the XIX century and weathering action in the Mercado do Ver-o-Peso building, northern Brazil: Identification with the usage of laboratory analysis

Palácios, Flávia Olegário, Angélica, Rômulo Simões, Sanjad, Thais Alessandra Bastos Caminha

Journal:

Materials Characterization

Year:

2014

Language:

english

File:

PDF, 2.04 MB

english, 2014

37

10.1038/79208

Karet, Fiona E., Smith, Annabel N., Skaug, Jennifer, Choate, Keith A., Nayir, Ahmet, Bakkaloglu, Aysin, Ozen, Seza, Hulton, Sally A., Sanjad, Sami A., Al-Sabban, Essam A., Lifton, Richard P., Scherer,

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 693 KB

english, 2000

38

10.1038/5022

Karet, Fiona E., Finberg, Karin E., Nelson, Raoul D., Nayir, Ahmet, Mocan, Hilal, Sanjad, Sami A., Rodriguez-Soriano, Juan, Santos, Fernando, Cremers, Cor W.R.J., Pietro, Antonio Di, Hoffbrand, Barry

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 282 KB

english, 1999

39

Improved primary transplant success rates using a triple regimen of cyclosporine microemulsion, mycophenolate mofetil and prednisone

R.B Khauli, W.A Medawar, A.A Habbal, A.E Birbari, M.M Daouk, A.M Abdelnoor, M Uwaydah, A Rahman Bizri, S Sanjad, P.J Ayvazian, T Lovewell, J.S Stoff, P Yang Fan, P Bigwood, R Harland

Journal:

Transplantation Proceedings

Year:

2001

Language:

english

File:

PDF, 61 KB

english, 2001

40

Ureteropelvic Junction Obstruction and Parathyroid Adenoma: Coincidence or Link?

Termos, Salah, AlKabbani, Majd, Ulinski, Tim, Sanjad, Sami, Kotobi, Henri, Chalard, Francois, Aoun, Bilal

Journal:

Case Reports in Nephrology

Year:

2017

Language:

english

File:

PDF, 1.61 MB

english, 2017

41

Lime-based restoration paints: characterization and evaluation of formulations using a native species from the Amazon flora and PVA-based glue as additives

Silva, Mayra Martins, Sanjad, Thais Alessandra Bastos Caminha, Costa, Marcondes Lima da, Costa, Solange do Perpétuo Socorro Evangelista

Journal:

Ambiente Construído

Year:

2017

File:

PDF, 975 KB

2017

42

A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity

B. Burwinkel, S.A. Sanjad, E. Al-Sabban, A. Al-Abbad, M.W. Kilimann

Journal:

Year:

1999

Language:

english

File:

PDF, 77 KB

english, 1999

43

Sanjad-Sakati and autosomal recessive Kenny-Caffey syndromes are allelic: Evidence for an ancestral founder mutation and locus refinement

Diaz, G.A., Gelb, B.D., Ali, F., Sakati, N., Sanjad, S., Meyer, B.F., Kambouris, M.

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 115 KB

english, 1999

44

19th century stained-glass windows from Belém do Pará (Brazil): Analytical characterisation and pathology

Corrêa Pinto, Amanda M., Sanjad, Thais A.B.C., Angélica, Rômulo S., da Costa, Marcondes L., Paiva, Rosildo S., Palomar, Teresa

Journal:

Boletín de la Sociedad Española de Cerámica y Vidrio

Year:

2017

File:

PDF, 2.58 MB

2017

45

Kidney and Metabolic Phenotypes in Glycogen Storage Disease Type-I Patients

Aoun, Bilal, Sanjad, Sami, Degheili, Jad A., Barhoumi, Abir, Bassyouni, Amina, Karam, Pascale E.

Journal:

Frontiers in Pediatrics

Year:

2020

File:

PDF, 182 KB

2020

46

Renal venous thrombosis in a newborn with prothrombotic risk factors

Muwakkit, Samar A, Saab, Raya, Sanjad, Sami A, Bhar, Saleh I, Ishak, Rim S, Samad, Zeina A, Chan, Anthony K, Abboud, Miguel R

Journal:

Blood Coagulation & Fibrinolysis

Year:

2009

Language:

english

File:

PDF, 126 KB

english, 2009

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