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1

Inherited metabolic disorders in adults: A view from Saudi Arabia

Sulaiman, Raashda A., Al-Owain, Mohammed

Journal:

European Journal of Medical Genetics

Year:

2018

Language:

english

File:

PDF, 1.07 MB

english, 2018

2

First define impaired fasting glycaemia

Raashda Sulaiman and Mourad Labib

Journal:

Year:

2010

Language:

english

File:

PDF, 310 KB

english, 2010

3

Pitfalls in cerebrospinal fluid spectroscopy results for the diagnosis of subarachnoid haemorrhage

Sulaiman, Raashda A., Gama, Rousseau

Journal:

British Journal of Neurosurgery

Year:

2010

Language:

english

File:

PDF, 50 KB

english, 2010

4

Ethnic differences in umbilical cord blood vitamin D and parathyroid hormone – South Asians compared to Whites born in the UK

Sulaiman, Raashda A., Sharratt, Caroline L., Lee, Pek-wan, Skinner, Alyson, Griffiths, Melanie J., Webster, Craig, Ford, Clare, Anderson, Janet, Gama, Rousseau

Journal:

Journal of Maternal-Fetal and Neonatal Medicine

Year:

2010

Language:

english

File:

PDF, 153 KB

english, 2010

5

A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia

Caridi, Gianluca, Dagnino, Monica, Di Duca, Marco, Santra, Saikat, Ball, Sarah, Sulaiman, Raashda A., Campagnoli, Monica, Galliano, Monica, Minchiotti, Lorenzo

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

2012

Language:

english

File:

PDF, 110 KB

english, 2012

6

Autozygosity reveals recessive mutations and novel mechanisms in dominant genes: implications in variant interpretation

Monies, Dorota, Maddirevula, Sateesh, Kurdi, Wesam, Alanazy, Mohammed H., Alkhalidi, Hisham, Al-Owain, Mohammed, Sulaiman, Raashda A., Faqeih, Eissa, Goljan, Ewa, Ibrahim, Niema, Abdulwahab, Firdous,

Journal:

Genetics in Medicine

Year:

2017

Language:

english

File:

PDF, 1.15 MB

english, 2017

7

Juvenile hemochromatosis and hepatocellular carcinoma in a patient with a novel mutation in the HJV gene

Ramzan, Khushnooda, Imtiaz, Faiqa, Al-Ashgar, Hamad I., AlSayed, Moeenaldeen, Sulaiman, Raashda A.

Journal:

European Journal of Medical Genetics

Year:

2017

Language:

english

File:

PDF, 642 KB

english, 2017

8

[JIMD Reports] || Successful Management of Pregnancies in Patients with Inherited Disorders of Ketone Body Metabolism

Sulaiman, Raashda Ainuddin

Year:

2017

Language:

english

File:

PDF, 86 KB

english, 2017

9

Paraprotein interferences in routine laboratory assays

Sulaiman, Raashda, Othonos, Nanthia, Gama, Rousseau

Journal:

Year:

2011

Language:

english

File:

PDF, 45 KB

english, 2011

10

Pasireotide and octreotide in the treatment of severe late dumping syndrome

Mohammadi, Alireza, Sulaiman, Raashda A., Grossman, Ashley B.

Journal:

Clinical Case Reports

Year:

2017

Language:

english

File:

PDF, 72 KB

english, 2017

11

CORRIGENDUM: Autozygosity reveals recessive mutations and novel mechanisms in dominant genes: implications in variant interpretation

Monies, Dorota, Maddirevula, Sateesh, Kurdi, Wesam, Alanazy, Mohammed H, Alkhalidi, Hisham, Al-Owain, Mohammed, Sulaiman, Raashda A, Faqeih, Eissa, Goljan, Ewa, Ibrahim, Niema, Abdulwahab, Firdous, Ha

Journal:

Genetics in Medicine

Year:

2018

Language:

english

File:

PDF, 49 KB

english, 2018

12

Biotin treatment causing erroneous immunoassay results: A word of caution for clinicians

Sulaiman, Raashda Ainuddin

Journal:

Drug Discoveries & Therapeutics

Year:

2016

Language:

english

File:

PDF, 161 KB

english, 2016

13

Depression in adult patients with biotin responsive basal ganglia disease

Bubshait, Dalal K., Rashid, Asif, Al-Owain, Mohammed A., Sulaiman, Raashda A.

Journal:

Drug Discoveries & Therapeutics

Year:

2016

Language:

english

File:

PDF, 982 KB

english, 2016

14

Optic neuropathy in classical methylmalonic acidemia

AlOwain, Mohammed, Khalifa, Ola Ali, Al Sahlawi, Zahra, Hussein, Maged H, Sulaiman, Raashda A, Al-Sayed, Moeen, Rahbeeni, Zuhair, Al-Hassnan, Zuhair, Al-Zaidan, Hamad, Nezzar, Hachemi, Al Homoud, Ifte

Journal:

Ophthalmic Genetics

Year:

2019

Language:

english

File:

PDF, 1.52 MB

english, 2019

15

Inherited metabolic disorders and dyslipidaemia

Sulaiman, Raashda A

Journal:

Journal of Clinical Pathology

Year:

2019

Language:

english

File:

PDF, 1.19 MB

english, 2019

16

Inherited metabolic disorders and dyslipidaemia

Sulaiman, Raashda A

Journal:

Journal of Clinical Pathology

Year:

2019

File:

PDF, 1.19 MB

2019

17

Hemophagocytic lymphohistiocytosis: A rare cause of recurrent encephalopathy

Sulaiman, Raashda Ainuddin, Shaheen, Marwan Yassin, Al-Zaidan, Hamad, Al-Hassnan, Zuhair, Al-Sayed, Moeenaldeen, Rahbeeni, Zuhair, Bakshi, Nasir Ahmed, Kaya, Namik, Aldosary, Mazhor, Al-Owain, Mohamme

Journal:

Intractable & Rare Diseases Research

Year:

2016

Language:

english

File:

PDF, 421 KB

english, 2016

18

The neuroimaging findings of monocarboxylate transporter 1 deficiency

Nicolas-Jilwan, Manal, Medlej, Rita, Sulaiman, Raashda A, AlSayed, Moeenaldeen

Journal:

Year:

2020

File:

PDF, 339 KB

2020

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