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1

Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia

K Brakensiek, H Frye-Boukhriss, M Mälzer, M Abramowicz, MJ Bahr, N Von Beckerath, C Bergmann, M Caselitz, E Holinski-Feder, P Muschke, K Oexle, G Strobl-Wildemann, G Wolff, EA El-Harith, M Stuhrmann

Journal:

Clinical Genetics

Year:

2008

Language:

english

File:

PDF, 103 KB

english, 2008

2

Hepatic manifestation is associated with ALK1 in hereditary hemorrhagic telangiectasia: Identification of five novel ALK1 and one novel ENG mutations

Heidi K.A. Kuehl, Martin Caselitz, Sandra Hasenkamp, Siegfried Wagner, El-Harith A. El-Harith, Michael P. Manns, Manfred Stuhrmann

Journal:

Year:

2005

Language:

english

File:

PDF, 123 KB

english, 2005

3

Some factors influencing caecal enlargement induced by raw potato starch in the rat

E.A. El-Harith, R. Walker, G.G. Birch, G. Sukan

Journal:

Year:

1977

Language:

english

File:

PDF, 524 KB

english, 1977

4

On the nutritive value of various starches for the albino rat

El-Harith A. El-Harith, John W. T. Dickerson, Ronald Walker

Journal:

Journal of the Science of Food and Agriculture

Year:

1976

Language:

english

File:

PDF, 343 KB

english, 1976

5

Diagnosis of Xeroderma pigmentosum C by detection of the founder mutation c.1643_1644delTG (p.Val548Ala fsX25) in a Sudanese Family

El-Harith A. El-Harith, Lisa Pahl, Khlood Al-Nutaifi, Iqbal Bukhari, Joerg Schmidtke, Manfred Stuhrmann

Journal:

Journal of the Saudi Society of Dermatology & Dermatologic Surgery

Year:

2012

Language:

english

File:

PDF, 286 KB

english, 2012

6

Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23

M Stuhrmann, HC Hennies, IA Bukhari, K Brakensiek, G Nürnberg, C Becker, J Huebener, MC Miranda, H Frye-Boukhriss, S Knothe, J Schmidtke, E-HA El-Harith

Journal:

Clinical Genetics

Year:

2008

Language:

english

File:

PDF, 422 KB

english, 2008

7

Potato starch and caecal hypertrophy in the rat

E.A. El-Harith, J.W.T. Dickerson, R. Walker

Journal:

Food and Cosmetics Toxicology

Year:

1976

Language:

english

File:

PDF, 4.25 MB

english, 1976

8

The β-globin genotype E121Q/W15X (cd121GAA→CAA/cd15TGG→TGA) underlines Hb

M. Ahmed, M. Stuhrmann, L. Bashawri, W. Kühnau, El-Harith A. EL-Harith

Journal:

Annals of Hematology

Year:

2001

Language:

english

File:

PDF, 40 KB

english, 2001

9

The Effect of Reduced Ambient Temperature on the Metabolism of some 14C-isotopelabeled Fatty Acids and 14C-Glucose by the Rat's Brown Adipose Tissue

E. A. El-harith, U. ter Meulen

Journal:

Journal of Animal Physiology and Animal Nutrition

Year:

1980

Language:

english

File:

PDF, 424 KB

english, 1980

10

Hereditary hemorrhagic telangiectasia is caused by the Q490X mutation of the ACVRL1 gene in a large Arab family: support of homozygous lethality

El-Harith A. El-Harith, Wolfgang Kühnau, Jörg Schmidtke, Dorothea Gadzicki, Mirghani Ahmed, Michael Krawczak, Manfred Stuhrmann

Journal:

European Journal of Medical Genetics

Year:

2006

Language:

english

File:

PDF, 243 KB

english, 2006

11

Familial thrombocytosis as a recessive, possibly X-linked trait in an Arab family

M Stuhrmann, L. Bashawri, M. A. Ahmed, B. H. Al-Awamy, W. Kühnau, J. Schmidtke, E. A. El-Harith

Journal:

British Journal of Haematology

Year:

2001

Language:

english

File:

PDF, 110 KB

english, 2001

12

Effects of mimosine on some serum enzyme activities and amino acid metabolism in the rat

E. A. El-Harith, H. Mohme, U. ter Meulen, Monika Bartha, K.-D. Günther

Journal:

Journal of Animal Physiology and Animal Nutrition

Year:

1981

Language:

english

File:

PDF, 425 KB

english, 1981

13

A case of diffuse cutaneous leishmaniasis due to Leishmania major

Ahmed Awad Abdel-Hameed, Bushra Omer Ahmed, Ahmed Abdalla Mohamedani, Abdalla El-Harith, Guillaume Van Eys

Journal:

Transactions of the Royal Society of Tropical Medicine and Hygiene

Year:

1990

Language:

english

File:

PDF, 464 KB

english, 1990

14

Metabolic effects of mimosine on tyrosine in the rat

U. ter Meulen, K.-D. Günther, E. A. El-Harith

Journal:

Journal of Animal Physiology and Animal Nutrition

Year:

1981

Language:

english

File:

PDF, 295 KB

english, 1981

15

Familial thrombocytosis caused by the novel germ-line mutation p.Pro106Leu in the MPL gene

El-Harith Abdelghaffar El-Harith, Cornelia Roesl, Matthias Ballmaier, Manuela Germeshausen, Hildegard Frye-Boukhriss, Nils Von Neuhoff, Christian Becker, Gudrun Nürnberg, Peter Nürnberg, Mirghani Ali

Journal:

British Journal of Haematology

Year:

2009

Language:

english

File:

PDF, 302 KB

english, 2009

16

Evidence for a Common Ethnic Origin of Cystic Fibrosis Mutation 3120+1G→A in Diverse Populations

Thilo Dörk, El-Harith A. El-Harith, Manfred Stuhrmann, Milan Macek Jr., Michelle Egan, Garry R. Cutting, Maria Tzetis, Emmanuel Kanavakis, Soukeyna Carles, Mireille Claustres, Carolyn Padoa, Michèle R

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 291 KB

english, 1998

17

Pre-Eclampsia: Maternal Risk Factors and Perinatal Outcome

Al-Mulhim, Abdul-Aziz, Abu-Heija, Adel, Al-Jamma, Fathia, El-Harith, El-Harith A.

Journal:

Fetal Diagnosis and Therapy

Year:

2003

Language:

english

File:

PDF, 96 KB

english, 2003

18

Vascular endothelial growth factor A polymorphism and risk of Kaposi's sarcoma herpesvirus viremia in kidney allograft recipients

Alkharsah, K.R., Alzahrani, A.J., Obeid, O.E., El-Harith, E.-H.A., Guella, A., Mohamed, E.A., Haykal, A.H., Stuhrmann, M., Al-Ali, A.K.

Journal:

Transplant Infectious Disease

Year:

2014

Language:

english

File:

PDF, 100 KB

english, 2014

19

Novel and characteristic CFTR mutations in Saudi Arab children with severe cystic fibrosis.

el-Harith, E A, Dork, T, Stuhrmann, M, Abu-Srair, H, al-Shahri, A, Keller, K M, Lentze, M J, Schmidtke, J

Journal:

Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 804 KB

english, 1997

20

Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family

IA Bukhari, EA EL-Harith, M Stuhrmann

Journal:

Journal of the European Academy of Dermatology and Venereology

Year:

2006

Language:

english

File:

PDF, 124 KB

english, 2006

21

The effect of administration of glycine and tyrosine on the growth depression caused by mimosine in Rats

E. A. El-Harith, Angelika Hiller, U. Ter Meulen

Journal:

Journal of Animal Physiology and Animal Nutrition

Year:

1983

Language:

english

File:

PDF, 335 KB

english, 1983

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